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rs869312768

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869312768(-;-)
Make rs869312768(-;TT)
Make rs869312768(TT;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47429867
GeneMSH2
is asnp
is mentioned by
dbSNPrs869312768
ebirs869312768
HLIrs869312768
Exacrs869312768
Varsomers869312768
Maprs869312768
PheGenIrs869312768
hapmaprs869312768
1000 genomesrs869312768
hgdprs869312768
ensemblrs869312768
gopubmedrs869312768
geneviewrs869312768
scholarrs869312768
googlers869312768
pharmgkbrs869312768
gwascentralrs869312768
openSNPrs869312768
23andMers869312768
23andMe allrs869312768
SNP Nexus

SNPshotrs869312768
SNPdbers869312768
MSV3drs869312768
GWAS Ctlgrs869312768
Max Magnitude0
ClinVar
Risk rs869312768(TT;TT)
Alt rs869312768(TT;TT)
Reference rs869312768(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47657005_47657006dupTT
CLNSRC
CLNACC RCV000210102.1,