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rs775802030

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs775802030(A;G)
Make rs775802030(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position31067089
GeneWRN
is asnp
is mentioned by
dbSNPrs775802030
ebirs775802030
HLIrs775802030
Exacrs775802030
Varsomers775802030
Maprs775802030
PheGenIrs775802030
hapmaprs775802030
1000 genomesrs775802030
hgdprs775802030
ensemblrs775802030
gopubmedrs775802030
geneviewrs775802030
scholarrs775802030
googlers775802030
pharmgkbrs775802030
gwascentralrs775802030
openSNPrs775802030
23andMers775802030
23andMe allrs775802030
SNP Nexus

SNPshotrs775802030
SNPdbers775802030
MSV3drs775802030
GWAS Ctlgrs775802030
Max Magnitude0
ClinVar
Risk rs775802030(G;G)
Alt rs775802030(G;G)
Reference rs775802030(A;A)
Significance Pathogenic
Disease Werner syndrome
Variation info
Gene WRN
CLNDBN Werner syndrome
Reversed 0
HGVS NC_000008.10:g.30924605A>G
CLNSRC
CLNACC RCV000179333.1,