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rs121908448

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908448(A;T)
Make rs121908448(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position31090843
GeneWRN
is asnp
is mentioned by
dbSNPrs121908448
ebirs121908448
HLIrs121908448
Exacrs121908448
Varsomers121908448
Maprs121908448
PheGenIrs121908448
hapmaprs121908448
1000 genomesrs121908448
hgdprs121908448
ensemblrs121908448
gopubmedrs121908448
geneviewrs121908448
scholarrs121908448
googlers121908448
pharmgkbrs121908448
gwascentralrs121908448
openSNPrs121908448
23andMers121908448
23andMe allrs121908448
SNP Nexus

SNPshotrs121908448
SNPdbers121908448
MSV3drs121908448
GWAS Ctlgrs121908448
Max Magnitude0
OMIM604611
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121908448(T;T)
Alt rs121908448(T;T)
Reference rs121908448(A;A)
Significance Pathogenic
Disease Werner syndrome
Variation info
Gene WRN
CLNDBN Werner syndrome
Reversed 0
HGVS NC_000008.10:g.30948359A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005785.2,