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rs1060502023

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060502023(C;C)
Make rs1060502023(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47463156
GeneMSH2
is asnp
is mentioned by
dbSNPrs1060502023
dbSNP (classic)rs1060502023
ClinGenrs1060502023
ebirs1060502023
HLIrs1060502023
Exacrs1060502023
Gnomadrs1060502023
Varsomers1060502023
LitVarrs1060502023
Maprs1060502023
PheGenIrs1060502023
Biobankrs1060502023
1000 genomesrs1060502023
hgdprs1060502023
ensemblrs1060502023
geneviewrs1060502023
scholarrs1060502023
googlers1060502023
pharmgkbrs1060502023
gwascentralrs1060502023
openSNPrs1060502023
23andMers1060502023
23andMe allrs1060502023
SNPshotrs1060502023
SNPdbers1060502023
MSV3drs1060502023
GWAS Ctlgrs1060502023
Max Magnitude0
ClinVar
Risk rs1060502023(C;C)
Alt rs1060502023(C;C)
Reference Rs1060502023(T;T)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47690295T>C
CLNSRC
CLNACC RCV000461276.1, RCV000491134.1,