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rs121908447

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908447(C;T)
Make rs121908447(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position31147397
GeneWRN
is asnp
is mentioned by
dbSNPrs121908447
ebirs121908447
HLIrs121908447
Exacrs121908447
Varsomers121908447
Maprs121908447
PheGenIrs121908447
hapmaprs121908447
1000 genomesrs121908447
hgdprs121908447
ensemblrs121908447
gopubmedrs121908447
geneviewrs121908447
scholarrs121908447
googlers121908447
pharmgkbrs121908447
gwascentralrs121908447
openSNPrs121908447
23andMers121908447
23andMe allrs121908447
SNP Nexus

SNPshotrs121908447
SNPdbers121908447
MSV3drs121908447
GWAS Ctlgrs121908447
Max Magnitude0
OMIM604611
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908447(T;T)
Alt rs121908447(T;T)
Reference rs121908447(C;C)
Significance Pathogenic
Disease Werner syndrome
Variation info
Gene WRN
CLNDBN Werner syndrome
Reversed 0
HGVS NC_000008.10:g.31004913C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005778.3,