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rs876657675

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657675(C;C)
Make rs876657675(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position6302303
GeneWFS1
is asnp
is mentioned by
dbSNPrs876657675
ebirs876657675
HLIrs876657675
Exacrs876657675
Varsomers876657675
Maprs876657675
PheGenIrs876657675
hapmaprs876657675
1000 genomesrs876657675
hgdprs876657675
ensemblrs876657675
gopubmedrs876657675
geneviewrs876657675
scholarrs876657675
googlers876657675
pharmgkbrs876657675
gwascentralrs876657675
openSNPrs876657675
23andMers876657675
23andMe allrs876657675
SNP Nexus

SNPshotrs876657675
SNPdbers876657675
MSV3drs876657675
GWAS Ctlgrs876657675
Max Magnitude0
ClinVar
Risk rs876657675(C;C)
Alt rs876657675(C;C)
Reference rs876657675(G;G)
Significance Probable-Pathogenic
Disease WFS1-Related Disorders
Variation info
Gene WFS1
CLNDBN WFS1-Related Disorders
Reversed 0
HGVS NC_000004.11:g.6304030G>C
CLNSRC
CLNACC RCV000219504.1,