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rs606231162

From SNPedia

Orientationplus
Geno Mag Summary
(AGAC;AGAC) 0 common in clinvar
Make rs606231162(-;-)
Make rs606231162(-;AGAC)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position31154626
GeneLOC105379359, WRN
is asnp
is mentioned by
dbSNPrs606231162
ebirs606231162
HLIrs606231162
Exacrs606231162
Varsomers606231162
Maprs606231162
PheGenIrs606231162
hapmaprs606231162
1000 genomesrs606231162
hgdprs606231162
ensemblrs606231162
gopubmedrs606231162
geneviewrs606231162
scholarrs606231162
googlers606231162
pharmgkbrs606231162
gwascentralrs606231162
openSNPrs606231162
23andMers606231162
23andMe allrs606231162
SNP Nexus

SNPshotrs606231162
SNPdbers606231162
MSV3drs606231162
GWAS Ctlgrs606231162
Max Magnitude0
ClinVar
Risk rs606231162(;)
Alt rs606231162(;)
Reference rs606231162(AGAC;AGAC)
Significance Pathogenic
Disease Werner syndrome
Variation info
Gene WRN
CLNDBN Werner syndrome
Reversed 0
HGVS NC_000008.10:g.31012142_31012145delAGAC
CLNSRC OMIM Allelic Variant
CLNACC RCV000005779.4,