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rs201239579

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201239579(G;T)
Make rs201239579(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6302049
GeneWFS1
is asnp
is mentioned by
dbSNPrs201239579
ebirs201239579
HLIrs201239579
Exacrs201239579
Varsomers201239579
Maprs201239579
PheGenIrs201239579
hapmaprs201239579
1000 genomesrs201239579
hgdprs201239579
ensemblrs201239579
gopubmedrs201239579
geneviewrs201239579
scholarrs201239579
googlers201239579
pharmgkbrs201239579
gwascentralrs201239579
openSNPrs201239579
23andMers201239579
23andMe allrs201239579
SNP Nexus

SNPshotrs201239579
SNPdbers201239579
MSV3drs201239579
GWAS Ctlgrs201239579
Max Magnitude0
ClinVar
Risk rs201239579(T;T)
Alt rs201239579(T;T)
Reference rs201239579(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6303776G>T
CLNSRC
CLNACC RCV000195490.1,