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rs121908446

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908446(C;T)
Make rs121908446(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position31157461
GeneWRN
is asnp
is mentioned by
dbSNPrs121908446
ebirs121908446
HLIrs121908446
Exacrs121908446
Varsomers121908446
Maprs121908446
PheGenIrs121908446
hapmaprs121908446
1000 genomesrs121908446
hgdprs121908446
ensemblrs121908446
gopubmedrs121908446
geneviewrs121908446
scholarrs121908446
googlers121908446
pharmgkbrs121908446
gwascentralrs121908446
openSNPrs121908446
23andMers121908446
23andMe allrs121908446
SNP Nexus

SNPshotrs121908446
SNPdbers121908446
MSV3drs121908446
GWAS Ctlgrs121908446
Max Magnitude0
OMIM604611
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908446(T;T)
Alt rs121908446(T;T)
Reference rs121908446(C;C)
Significance Pathogenic
Disease Werner syndrome
Variation info
Gene WRN
CLNDBN Werner syndrome
Reversed 0
HGVS NC_000008.10:g.31014977C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005777.2,