chr1:157670816:A>G Detail (hg19)

Information

Genome

Assembly Position
hg19 chr1:157,670,816-157,670,816
hg38 chr1:157,701,026-157,701,026 View the variant detail on this assembly version.

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.383
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.213 rheumatoid arthritis No associations were found for rs1800795 (IL-6), rs1800896 (IL-10) and rs7528684... BeFree 25566937 Detail
0.035 rheumatoid arthritis No associations were found for rs1800795 (IL-6), rs1800896 (IL-10) and rs7528684... BeFree 25566937 Detail
0.203 rheumatoid arthritis No associations were found for rs1800795 (IL-6), rs1800896 (IL-10) and rs7528684... BeFree 25566937 Detail
0.145 Graves Disease The AA genotype of PTPN22 rs3789604 and AA genotype of FCRL3 rs7528684 were corr... BeFree 19438904 Detail
<0.001 neuromyelitis optica The Fc Receptor-Like 3 Polymorphisms (rs7528684, rs945635, rs3761959 and rs22822... BeFree 26402798 Detail
0.228 Graves Disease These preliminary results demonstrate that the immune-regulatory gene CTLA-4 and... BeFree 19438904 Detail
0.035 rheumatoid arthritis We found some evidence for an association of either rs7528684/fcrl3_3 or rs37928... BeFree 18087673 Detail
0.249 Graves Disease Above data indicated that FCRL3 gene and its proxy SNP rs7528684 may be involved... BeFree 23505439 Detail
0.010 Diabetes Mellitus, Insulin-Dependent [Genome-wide association analysis of autoantibody positivity in type 1 diabetes ... GAD 21829393 Detail
0.013 Autoimmune Diseases The Fcrl3 -169T&gt;C (rs7528684) polymorphism has been shown to be a risk factor... BeFree 24593204 Detail
0.234 ulcerative colitis Our aim was to study the role of two promoter SNPs of the FCRL3 gene (-169A&gt;G... BeFree 17389014 Detail
0.010 Inflammatory Bowel Diseases Our aim was to study the role of two promoter SNPs of the FCRL3 gene (-169A&gt;G... BeFree 17389014 Detail
0.397 Inflammatory Bowel Diseases Our aim was to study the role of two promoter SNPs of the FCRL3 gene (-169A&gt;G... BeFree 17389014 Detail
Annotation

Annotations

DescrptionSourceLinks
No associations were found for rs1800795 (IL-6), rs1800896 (IL-10) and rs7528684 (FCRL3) in the tota... DisGeNET Detail
No associations were found for rs1800795 (IL-6), rs1800896 (IL-10) and rs7528684 (FCRL3) in the tota... DisGeNET Detail
No associations were found for rs1800795 (IL-6), rs1800896 (IL-10) and rs7528684 (FCRL3) in the tota... DisGeNET Detail
The AA genotype of PTPN22 rs3789604 and AA genotype of FCRL3 rs7528684 were correlated with a reduce... DisGeNET Detail
The Fc Receptor-Like 3 Polymorphisms (rs7528684, rs945635, rs3761959 and rs2282284) and The Risk of ... DisGeNET Detail
These preliminary results demonstrate that the immune-regulatory gene CTLA-4 and the thyroid-specifi... DisGeNET Detail
We found some evidence for an association of either rs7528684/fcrl3_3 or rs3792876/slc2F2 with RA; h... DisGeNET Detail
Above data indicated that FCRL3 gene and its proxy SNP rs7528684 may be involved in the pathogenesis... DisGeNET Detail
[Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.] DisGeNET Detail
The Fcrl3 -169T&gt;C (rs7528684) polymorphism has been shown to be a risk factor of various autoimmu... DisGeNET Detail
Our aim was to study the role of two promoter SNPs of the FCRL3 gene (-169A&gt;G, rs7528684 and -110... DisGeNET Detail
Our aim was to study the role of two promoter SNPs of the FCRL3 gene (-169A&gt;G, rs7528684 and -110... DisGeNET Detail
Our aim was to study the role of two promoter SNPs of the FCRL3 gene (-169A&gt;G, rs7528684 and -110... DisGeNET Detail
Gene
-
dbSNP
rs7528684 dbSNP
Genome
hg19
Position
chr1:157,670,816-157,670,816
Variant Type
snv
Reference Allele
A
Alternative Allele
G
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs7528684
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.383
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
6419
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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