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rs71539673

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs71539673(A;A)
Make rs71539673(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6302220
GeneWFS1
is asnp
is mentioned by
dbSNPrs71539673
ebirs71539673
HLIrs71539673
Exacrs71539673
Varsomers71539673
Maprs71539673
PheGenIrs71539673
hapmaprs71539673
1000 genomesrs71539673
hgdprs71539673
ensemblrs71539673
gopubmedrs71539673
geneviewrs71539673
scholarrs71539673
googlers71539673
pharmgkbrs71539673
gwascentralrs71539673
openSNPrs71539673
23andMers71539673
23andMe allrs71539673
SNP Nexus

SNPshotrs71539673
SNPdbers71539673
MSV3drs71539673
GWAS Ctlgrs71539673
Max Magnitude0
ClinVar
Risk rs71539673(A;A)
Alt rs71539673(A;A)
Reference rs71539673(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6303947G>A
CLNSRC
CLNACC RCV000200584.1,