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rs587776621

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776621(-;-)
Make rs587776621(-;A)
Make rs587776621(A;A)
ReferenceGRCh38 38.1/142
Chromosome8
Position31157463
GeneWRN
is asnp
is mentioned by
dbSNPrs587776621
ebirs587776621
HLIrs587776621
Exacrs587776621
Varsomers587776621
Maprs587776621
PheGenIrs587776621
hapmaprs587776621
1000 genomesrs587776621
hgdprs587776621
ensemblrs587776621
gopubmedrs587776621
geneviewrs587776621
scholarrs587776621
googlers587776621
pharmgkbrs587776621
gwascentralrs587776621
openSNPrs587776621
23andMers587776621
23andMe allrs587776621
SNP Nexus

SNPshotrs587776621
SNPdbers587776621
MSV3drs587776621
GWAS Ctlgrs587776621
Max Magnitude0
ClinVar
Risk rs587776621(A;A)
Alt rs587776621(A;A)
Reference rs587776621(;)
Significance Pathogenic
Disease Werner syndrome
Variation info
Gene WRN
CLNDBN Werner syndrome
Reversed 0
HGVS NC_000008.10:g.31014979dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000005781.2,