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rs71537685

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs71537685(A;A)
Make rs71537685(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position6300657
GeneWFS1
is asnp
is mentioned by
dbSNPrs71537685
ebirs71537685
HLIrs71537685
Exacrs71537685
Varsomers71537685
Maprs71537685
PheGenIrs71537685
hapmaprs71537685
1000 genomesrs71537685
hgdprs71537685
ensemblrs71537685
gopubmedrs71537685
geneviewrs71537685
scholarrs71537685
googlers71537685
pharmgkbrs71537685
gwascentralrs71537685
openSNPrs71537685
23andMers71537685
23andMe allrs71537685
SNP Nexus

SNPshotrs71537685
SNPdbers71537685
MSV3drs71537685
GWAS Ctlgrs71537685
Max Magnitude0
ClinVar
Risk rs71537685(A;A)
Alt rs71537685(A;A)
Reference rs71537685(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6302384G>A
CLNSRC
CLNACC RCV000171514.1,