chr6:31106253:A>C Detail (hg38)

Information

Genome

Assembly Position
hg19 chr6:31,074,030-31,074,030 View the variant detail on this assembly version.
hg38 chr6:31,106,253-31,106,253

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.583
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
0.001 Lymphoma, Follicular In recent genome-wide association studies (GWAS) of FL, several genetic suscepti... BeFree 23025665 Detail
0.005 Lymphoma, Follicular [Genome-wide association study of follicular lymphoma identifies a risk locus at... GAD 20639881 Detail
0.005 Lymphoma, Follicular [Genetic variants at 6p21.33 are associated with susceptibility to follicular ly... GAD 19620980 Detail
Annotation

Annotations

DescrptionSourceLinks
In recent genome-wide association studies (GWAS) of FL, several genetic susceptibility loci have bee... DisGeNET Detail
[Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.] DisGeNET Detail
[Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma.] DisGeNET Detail
Gene
-
dbSNP
rs6457327 dbSNP
Genome
hg38
Position
chr6:31,106,253-31,106,253
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))
rs6457327
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.5829
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
9770
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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