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rs797046113

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CCTCTT;CCTCTT) 0 common in clinvar
(CTTCCT;CTTCCT) 0 common in clinvar
Make rs797046113(-;-)
Make rs797046113(-;CCTCTT)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6301493
GeneWFS1
is asnp
is mentioned by
dbSNPrs797046113
dbSNP (old)rs797046113
ClinGenrs797046113
ebirs797046113
HLIrs797046113
Exacrs797046113
Varsomers797046113
Maprs797046113
PheGenIrs797046113
Biobankrs797046113
1000 genomesrs797046113
hgdprs797046113
ensemblrs797046113
gopubmedrs797046113
geneviewrs797046113
scholarrs797046113
googlers797046113
pharmgkbrs797046113
gwascentralrs797046113
openSNPrs797046113
23andMers797046113
23andMe allrs797046113
SNP Nexus

SNPshotrs797046113
SNPdbers797046113
MSV3drs797046113
GWAS Ctlgrs797046113
Max Magnitude0
ClinVar
Risk rs797046113(-;-) Rs797046113(CTTCCT;CTTCCT)
Alt rs797046113(-;-) Rs797046113(CTTCCT;CTTCCT)
Reference Rs797046113(CCTCTT;CCTCTT)
Significance Probable-Pathogenic
Disease Wolfram syndrome
Variation info
Gene WFS1
CLNDBN Wolfram syndrome
Reversed 0
HGVS NC_000004.11:g.6303220_6303225delCCTCTT
CLNSRC
CLNACC RCV000194382.1,