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rs863224266

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CG;CG) 0 common in clinvar
Make rs863224266(CG;TA)
Make rs863224266(TA;TA)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6301626
GeneWFS1
is asnp
is mentioned by
dbSNPrs863224266
dbSNP (old)rs863224266
ClinGenrs863224266
ebirs863224266
HLIrs863224266
Exacrs863224266
Varsomers863224266
Maprs863224266
PheGenIrs863224266
Biobankrs863224266
1000 genomesrs863224266
hgdprs863224266
ensemblrs863224266
gopubmedrs863224266
geneviewrs863224266
scholarrs863224266
googlers863224266
pharmgkbrs863224266
gwascentralrs863224266
openSNPrs863224266
23andMers863224266
23andMe allrs863224266
SNP Nexus

SNPshotrs863224266
SNPdbers863224266
MSV3drs863224266
GWAS Ctlgrs863224266
Max Magnitude0
ClinVar
Risk rs863224266(TA;TA)
Alt rs863224266(TA;TA)
Reference Rs863224266(CG;CG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6303353_6303354delCGinsTA
CLNSRC
CLNACC RCV000196564.1,