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rs1060501991

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501991(A;A)
Make rs1060501991(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47480695
GeneMSH2
is asnp
is mentioned by
dbSNPrs1060501991
dbSNP (old)rs1060501991
ClinGenrs1060501991
ebirs1060501991
HLIrs1060501991
Exacrs1060501991
Gnomadrs1060501991
Varsomers1060501991
Maprs1060501991
PheGenIrs1060501991
Biobankrs1060501991
1000 genomesrs1060501991
hgdprs1060501991
ensemblrs1060501991
gopubmedrs1060501991
geneviewrs1060501991
scholarrs1060501991
googlers1060501991
pharmgkbrs1060501991
gwascentralrs1060501991
openSNPrs1060501991
23andMers1060501991
23andMe allrs1060501991
SNPshotrs1060501991
SNPdbers1060501991
MSV3drs1060501991
GWAS Ctlgrs1060501991
Max Magnitude0
ClinVar
Risk rs1060501991(A;A)
Alt rs1060501991(A;A)
Reference Rs1060501991(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47707834G>A
CLNSRC
CLNACC RCV000465186.1,