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rs878854136

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878854136(-;-)
Make rs878854136(-;AT)
Make rs878854136(AT;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position31120341
GeneWRN
is asnp
is mentioned by
dbSNPrs878854136
ebirs878854136
HLIrs878854136
Exacrs878854136
Varsomers878854136
Maprs878854136
PheGenIrs878854136
hapmaprs878854136
1000 genomesrs878854136
hgdprs878854136
ensemblrs878854136
gopubmedrs878854136
geneviewrs878854136
scholarrs878854136
googlers878854136
pharmgkbrs878854136
gwascentralrs878854136
openSNPrs878854136
23andMers878854136
23andMe allrs878854136
SNP Nexus

SNPshotrs878854136
SNPdbers878854136
MSV3drs878854136
GWAS Ctlgrs878854136
Max Magnitude0
ClinVar
Risk rs878854136(TA;TA)
Alt rs878854136(TA;TA)
Reference rs878854136(;)
Significance Pathogenic
Disease Werner syndrome
Variation info
Gene WRN
CLNDBN Werner syndrome
Reversed 0
HGVS NC_000008.10:g.30977856_30977857dupAT
CLNSRC
CLNACC RCV000229897.1,