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rs267607008

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607008(A;G)
Make rs267607008(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position31064962
GeneWRN
is asnp
is mentioned by
dbSNPrs267607008
ebirs267607008
HLIrs267607008
Exacrs267607008
Varsomers267607008
Maprs267607008
PheGenIrs267607008
hapmaprs267607008
1000 genomesrs267607008
hgdprs267607008
ensemblrs267607008
gopubmedrs267607008
geneviewrs267607008
scholarrs267607008
googlers267607008
pharmgkbrs267607008
gwascentralrs267607008
openSNPrs267607008
23andMers267607008
23andMe allrs267607008
SNP Nexus

SNPshotrs267607008
SNPdbers267607008
MSV3drs267607008
GWAS Ctlgrs267607008
Max Magnitude0
ClinVar
Risk rs267607008(G;G)
Alt rs267607008(G;G)
Reference rs267607008(A;A)
Significance Pathogenic
Disease Werner syndrome
Variation info
Gene WRN
CLNDBN Werner syndrome
Reversed 0
HGVS NC_000008.10:g.30922478A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005786.2,