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rs1060500056

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs1060500056(-;-)
Make rs1060500056(-;AA)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position31065061
GeneWRN
is asnp
is mentioned by
dbSNPrs1060500056
dbSNP (old)rs1060500056
ClinGenrs1060500056
ebirs1060500056
HLIrs1060500056
Exacrs1060500056
Gnomadrs1060500056
Varsomers1060500056
Maprs1060500056
PheGenIrs1060500056
Biobankrs1060500056
1000 genomesrs1060500056
hgdprs1060500056
ensemblrs1060500056
gopubmedrs1060500056
geneviewrs1060500056
scholarrs1060500056
googlers1060500056
pharmgkbrs1060500056
gwascentralrs1060500056
openSNPrs1060500056
23andMers1060500056
23andMe allrs1060500056
SNPshotrs1060500056
SNPdbers1060500056
MSV3drs1060500056
GWAS Ctlgrs1060500056
Max Magnitude0
ClinVar
Risk rs1060500056(-;-)
Alt rs1060500056(-;-)
Reference Rs1060500056(AA;AA)
Significance Pathogenic
Disease Werner syndrome
Variation info
Gene WRN
CLNDBN Werner syndrome
Reversed 0
HGVS NC_000008.10:g.30922577_30922578delAA
CLNSRC
CLNACC RCV000472438.1,