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rs863224268

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
(TC;TC) 0 common in clinvar
Make rs863224268(-;-)
Make rs863224268(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6302438
GeneLOC107986257, WFS1
is asnp
is mentioned by
dbSNPrs863224268
dbSNP (old)rs863224268
ClinGenrs863224268
ebirs863224268
HLIrs863224268
Exacrs863224268
Varsomers863224268
Maprs863224268
PheGenIrs863224268
Biobankrs863224268
1000 genomesrs863224268
hgdprs863224268
ensemblrs863224268
gopubmedrs863224268
geneviewrs863224268
scholarrs863224268
googlers863224268
pharmgkbrs863224268
gwascentralrs863224268
openSNPrs863224268
23andMers863224268
23andMe allrs863224268
SNP Nexus

SNPshotrs863224268
SNPdbers863224268
MSV3drs863224268
GWAS Ctlgrs863224268
Max Magnitude0
ClinVar
Risk rs863224268(-;-) Rs863224268(TC;TC)
Alt rs863224268(-;-) Rs863224268(TC;TC)
Reference Rs863224268(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6304165_6304166delCT
CLNSRC
CLNACC RCV000199613.1,