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rs28937894

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28937894(C;T)
Make rs28937894(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position6301891
GeneWFS1
is asnp
is mentioned by
dbSNPrs28937894
ebirs28937894
HLIrs28937894
Exacrs28937894
Varsomers28937894
Maprs28937894
PheGenIrs28937894
hapmaprs28937894
1000 genomesrs28937894
hgdprs28937894
ensemblrs28937894
gopubmedrs28937894
geneviewrs28937894
scholarrs28937894
googlers28937894
pharmgkbrs28937894
gwascentralrs28937894
openSNPrs28937894
23andMers28937894
23andMe allrs28937894
SNP Nexus

SNPshotrs28937894
SNPdbers28937894
MSV3drs28937894
GWAS Ctlgrs28937894
Max Magnitude0
deafness
OMIM606201
DescDEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 6
Variant0016
Relatedalso
Neighborrs28937891
Distance12
Neighborrs28937893
Distance50


ClinVar
Risk rs28937894(T;T)
Alt rs28937894(T;T)
Reference rs28937894(C;C)
Significance Pathogenic
Disease WFS1-Related Disorders not specified
Variation info
Gene WFS1
CLNDBN WFS1-Related Disorders not specified
Reversed 0
HGVS NC_000004.11:g.6303618C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004780.3, RCV000238945.1,