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rs369158322

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs369158322(A;C)
Make rs369158322(C;C)
ReferenceGRCh38 38.1/142
Chromosome8
Position31150454
GeneWRN
is asnp
is mentioned by
dbSNPrs369158322
dbSNP (old)rs369158322
ClinGenrs369158322
ebirs369158322
HLIrs369158322
Exacrs369158322
Varsomers369158322
Maprs369158322
PheGenIrs369158322
Biobankrs369158322
1000 genomesrs369158322
hgdprs369158322
ensemblrs369158322
gopubmedrs369158322
geneviewrs369158322
scholarrs369158322
googlers369158322
pharmgkbrs369158322
gwascentralrs369158322
openSNPrs369158322
23andMers369158322
23andMe allrs369158322
SNP Nexus

SNPshotrs369158322
SNPdbers369158322
MSV3drs369158322
GWAS Ctlgrs369158322
Max Magnitude0
ClinVar
Risk rs369158322(C;C) rs369158322(T;T)
Alt rs369158322(C;C) rs369158322(T;T)
Reference Rs369158322(A;A)
Significance Pathogenic
Disease Werner syndrome
Variation info
Gene WRN
CLNDBN Werner syndrome
Reversed 0
HGVS NC_000008.10:g.31007970A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005783.3,