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rs28937895

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs28937895(A;A)
Make rs28937895(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position6302287
GeneWFS1
is asnp
is mentioned by
dbSNPrs28937895
ebirs28937895
HLIrs28937895
Exacrs28937895
Varsomers28937895
Maprs28937895
PheGenIrs28937895
hapmaprs28937895
1000 genomesrs28937895
hgdprs28937895
ensemblrs28937895
gopubmedrs28937895
geneviewrs28937895
scholarrs28937895
googlers28937895
pharmgkbrs28937895
gwascentralrs28937895
openSNPrs28937895
23andMers28937895
23andMe allrs28937895
SNP Nexus

SNPshotrs28937895
SNPdbers28937895
MSV3drs28937895
GWAS Ctlgrs28937895
Max Magnitude0
deafness
OMIM606201
DescDEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 6
Variant0017
Relatedalso
Neighborrs28937890
Distance321


ClinVar
Risk rs28937895(A;A)
Alt rs28937895(A;A)
Reference rs28937895(G;G)
Significance Pathogenic
Disease WFS1-Related Disorders not provided
Variation info
Gene WFS1
CLNDBN WFS1-Related Disorders not provided
Reversed 0
HGVS NC_000004.11:g.6304014G>A; NC_000004.11:g.6304014G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000004781.3, RCV000195950.1,