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rs1060502032

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502032(G;T)
Make rs1060502032(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47476522
GeneMSH2
is asnp
is mentioned by
dbSNPrs1060502032
dbSNP (old)rs1060502032
ClinGenrs1060502032
ebirs1060502032
HLIrs1060502032
Exacrs1060502032
Gnomadrs1060502032
Varsomers1060502032
LitVarrs1060502032
Maprs1060502032
PheGenIrs1060502032
Biobankrs1060502032
1000 genomesrs1060502032
hgdprs1060502032
ensemblrs1060502032
gopubmedrs1060502032
geneviewrs1060502032
scholarrs1060502032
googlers1060502032
pharmgkbrs1060502032
gwascentralrs1060502032
openSNPrs1060502032
23andMers1060502032
23andMe allrs1060502032
SNPshotrs1060502032
SNPdbers1060502032
MSV3drs1060502032
GWAS Ctlgrs1060502032
Max Magnitude0
ClinVar
Risk rs1060502032(T;T)
Alt rs1060502032(T;T)
Reference Rs1060502032(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703661G>T
CLNSRC
CLNACC RCV000460606.1,