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rs878854133

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878854133(-;-)
Make rs878854133(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position31058462
GeneWRN
is asnp
is mentioned by
dbSNPrs878854133
ebirs878854133
HLIrs878854133
Exacrs878854133
Varsomers878854133
Maprs878854133
PheGenIrs878854133
hapmaprs878854133
1000 genomesrs878854133
hgdprs878854133
ensemblrs878854133
gopubmedrs878854133
geneviewrs878854133
scholarrs878854133
googlers878854133
pharmgkbrs878854133
gwascentralrs878854133
openSNPrs878854133
23andMers878854133
23andMe allrs878854133
SNP Nexus

SNPshotrs878854133
SNPdbers878854133
MSV3drs878854133
GWAS Ctlgrs878854133
Max Magnitude0
ClinVar
Risk rs878854133(;)
Alt rs878854133(;)
Reference rs878854133(A;A)
Significance Pathogenic
Disease Werner syndrome
Variation info
Gene WRN
CLNDBN Werner syndrome
Reversed 0
HGVS NC_000008.10:g.30915978delA
CLNSRC
CLNACC RCV000233160.1,