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rs797046112

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TCT;TCT) 0 common in clinvar
Make rs797046112(-;-)
Make rs797046112(-;TTC)
Make rs797046112(TTC;TTC)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6301035
GeneWFS1
is asnp
is mentioned by
dbSNPrs797046112
dbSNP (old)rs797046112
ClinGenrs797046112
ebirs797046112
HLIrs797046112
Exacrs797046112
Gnomadrs797046112
Varsomers797046112
Maprs797046112
PheGenIrs797046112
Biobankrs797046112
1000 genomesrs797046112
hgdprs797046112
ensemblrs797046112
gopubmedrs797046112
geneviewrs797046112
scholarrs797046112
googlers797046112
pharmgkbrs797046112
gwascentralrs797046112
openSNPrs797046112
23andMers797046112
23andMe allrs797046112
SNP Nexus

SNPshotrs797046112
SNPdbers797046112
MSV3drs797046112
GWAS Ctlgrs797046112
Max Magnitude0
ClinVar
Risk rs797046112(-;-)
Alt rs797046112(-;-)
Reference Rs797046112(TCT;TCT)
Significance Probable-Pathogenic
Disease Wolfram syndrome
Variation info
Gene WFS1
CLNDBN Wolfram syndrome
Reversed 0
HGVS NC_000004.11:g.6302762_6302764delTTC
CLNSRC
CLNACC RCV000193337.1,