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rs71526458

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs71526458(C;T)
Make rs71526458(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6301989
GeneWFS1
is asnp
is mentioned by
dbSNPrs71526458
ebirs71526458
HLIrs71526458
Exacrs71526458
Varsomers71526458
Maprs71526458
PheGenIrs71526458
hapmaprs71526458
1000 genomesrs71526458
hgdprs71526458
ensemblrs71526458
gopubmedrs71526458
geneviewrs71526458
scholarrs71526458
googlers71526458
pharmgkbrs71526458
gwascentralrs71526458
openSNPrs71526458
23andMers71526458
23andMe allrs71526458
SNP Nexus

SNPshotrs71526458
SNPdbers71526458
MSV3drs71526458
GWAS Ctlgrs71526458
Max Magnitude0
ClinVar
Risk rs71526458(T;T)
Alt rs71526458(T;T)
Reference rs71526458(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6303716C>T
CLNSRC
CLNACC RCV000200446.2,