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rs149013740

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149013740(A;A)
Make rs149013740(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6301990
GeneWFS1
is asnp
is mentioned by
dbSNPrs149013740
ebirs149013740
HLIrs149013740
Exacrs149013740
Varsomers149013740
Maprs149013740
PheGenIrs149013740
hapmaprs149013740
1000 genomesrs149013740
hgdprs149013740
ensemblrs149013740
gopubmedrs149013740
geneviewrs149013740
scholarrs149013740
googlers149013740
pharmgkbrs149013740
gwascentralrs149013740
openSNPrs149013740
23andMers149013740
23andMe allrs149013740
SNP Nexus

SNPshotrs149013740
SNPdbers149013740
MSV3drs149013740
GWAS Ctlgrs149013740
Max Magnitude0
ClinVar
Risk rs149013740(A;A)
Alt rs149013740(A;A)
Reference rs149013740(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6303717G>A
CLNSRC
CLNACC RCV000197209.1,