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rs797045118

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs797045118(-;-)
Make rs797045118(-;GA)
Make rs797045118(GA;GA)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position31065046
GeneWRN
is asnp
is mentioned by
dbSNPrs797045118
dbSNP (old)rs797045118
ClinGenrs797045118
ebirs797045118
HLIrs797045118
Exacrs797045118
Varsomers797045118
Maprs797045118
PheGenIrs797045118
Biobankrs797045118
1000 genomesrs797045118
hgdprs797045118
ensemblrs797045118
gopubmedrs797045118
geneviewrs797045118
scholarrs797045118
googlers797045118
pharmgkbrs797045118
gwascentralrs797045118
openSNPrs797045118
23andMers797045118
23andMe allrs797045118
SNP Nexus

SNPshotrs797045118
SNPdbers797045118
MSV3drs797045118
GWAS Ctlgrs797045118
Max Magnitude0
ClinVar
Risk rs797045118(-;-)
Alt rs797045118(-;-)
Reference Rs797045118(AG;AG)
Significance Probable-Pathogenic
Disease Werner syndrome
Variation info
Gene WRN
CLNDBN Werner syndrome
Reversed 0
HGVS NC_000008.10:g.30922562_30922563delGA
CLNSRC
CLNACC RCV000190647.1,