chr7:128928906:A>C Detail (hg38)

Information

Genome

Assembly Position
hg19 chr7:128,568,960-128,568,960 View the variant detail on this assembly version.
hg38 chr7:128,928,906-128,928,906

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.282
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
0.235 Lupus Erythematosus, Systemic The IRF5 haplotype (rs729302 A, rs2004640 T, and rs2280714 T), which was reporte... BeFree 21239750 Detail
0.235 Lupus Erythematosus, Systemic [The genetic contribution towards predicting early-onset disease in patients wit... GAD 20881011 Detail
<0.001 rheumatoid arthritis A significant association of the rs729302 A allele with RA susceptibility was fo... BeFree 18408250 Detail
Annotation

Annotations

DescrptionSourceLinks
The IRF5 haplotype (rs729302 A, rs2004640 T, and rs2280714 T), which was reported as conferring an i... DisGeNET Detail
[The genetic contribution towards predicting early-onset disease in patients with SLE is quantified ... DisGeNET Detail
A significant association of the rs729302 A allele with RA susceptibility was found in both sets (od... DisGeNET Detail
Gene
-
dbSNP
rs729302 dbSNP
Genome
hg38
Position
chr7:128,928,906-128,928,906
Variant Type
snv
Reference Allele
A
Alternative Allele
C
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))
rs729302
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.2821
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
4727
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16758
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