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rs141585847

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs141585847(G;G)
Make rs141585847(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6301111
GeneWFS1
is asnp
is mentioned by
dbSNPrs141585847
ebirs141585847
HLIrs141585847
Exacrs141585847
Varsomers141585847
Maprs141585847
PheGenIrs141585847
hapmaprs141585847
1000 genomesrs141585847
hgdprs141585847
ensemblrs141585847
gopubmedrs141585847
geneviewrs141585847
scholarrs141585847
googlers141585847
pharmgkbrs141585847
gwascentralrs141585847
openSNPrs141585847
23andMers141585847
23andMe allrs141585847
SNP Nexus

SNPshotrs141585847
SNPdbers141585847
MSV3drs141585847
GWAS Ctlgrs141585847
Max Magnitude0
ClinVar
Risk rs141585847(G;G)
Alt rs141585847(G;G)
Reference rs141585847(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6302838T>G
CLNSRC
CLNACC RCV000199551.1,