Have questions? Visit https://www.reddit.com/r/SNPedia

rs878854131

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878854131(-;-)
Make rs878854131(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position31081192
GeneWRN
is asnp
is mentioned by
dbSNPrs878854131
ebirs878854131
HLIrs878854131
Exacrs878854131
Varsomers878854131
Maprs878854131
PheGenIrs878854131
hapmaprs878854131
1000 genomesrs878854131
hgdprs878854131
ensemblrs878854131
gopubmedrs878854131
geneviewrs878854131
scholarrs878854131
googlers878854131
pharmgkbrs878854131
gwascentralrs878854131
openSNPrs878854131
23andMers878854131
23andMe allrs878854131
SNP Nexus

SNPshotrs878854131
SNPdbers878854131
MSV3drs878854131
GWAS Ctlgrs878854131
Max Magnitude0
ClinVar
Risk rs878854131(;)
Alt rs878854131(;)
Reference rs878854131(A;A)
Significance Pathogenic
Disease Werner syndrome
Variation info
Gene WRN
CLNDBN Werner syndrome
Reversed 0
HGVS NC_000008.10:g.30938708delA
CLNSRC
CLNACC RCV000232269.1,