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rs387906337

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906337(A;T)
Make rs387906337(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position31064934
GeneWRN
is asnp
is mentioned by
dbSNPrs387906337
ebirs387906337
HLIrs387906337
Exacrs387906337
Varsomers387906337
Maprs387906337
PheGenIrs387906337
hapmaprs387906337
1000 genomesrs387906337
hgdprs387906337
ensemblrs387906337
gopubmedrs387906337
geneviewrs387906337
scholarrs387906337
googlers387906337
pharmgkbrs387906337
gwascentralrs387906337
openSNPrs387906337
23andMers387906337
23andMe allrs387906337
SNP Nexus

SNPshotrs387906337
SNPdbers387906337
MSV3drs387906337
GWAS Ctlgrs387906337
Max Magnitude0
ClinVar
Risk rs387906337(T;T)
Alt rs387906337(T;T)
Reference rs387906337(A;A)
Significance Pathogenic
Disease Werner syndrome
Variation info
Gene WRN
CLNDBN Werner syndrome
Reversed 0
HGVS NC_000008.10:g.30922450A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005786.2,