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rs1060501989

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501989(C;T)
Make rs1060501989(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47410115
GeneMSH2
is asnp
is mentioned by
dbSNPrs1060501989
dbSNP (old)rs1060501989
ClinGenrs1060501989
ebirs1060501989
HLIrs1060501989
Exacrs1060501989
Gnomadrs1060501989
Varsomers1060501989
Maprs1060501989
PheGenIrs1060501989
Biobankrs1060501989
1000 genomesrs1060501989
hgdprs1060501989
ensemblrs1060501989
gopubmedrs1060501989
geneviewrs1060501989
scholarrs1060501989
googlers1060501989
pharmgkbrs1060501989
gwascentralrs1060501989
openSNPrs1060501989
23andMers1060501989
23andMe allrs1060501989
SNPshotrs1060501989
SNPdbers1060501989
MSV3drs1060501989
GWAS Ctlgrs1060501989
Max Magnitude0
ClinVar
Risk rs1060501989(T;T)
Alt rs1060501989(T;T)
Reference Rs1060501989(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637254C>T
CLNSRC
CLNACC RCV000471483.1,