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rs794729229

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729229(A;A)
Make rs794729229(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47480696
GeneMSH2
is asnp
is mentioned by
dbSNPrs794729229
ebirs794729229
HLIrs794729229
Exacrs794729229
Varsomers794729229
Maprs794729229
PheGenIrs794729229
hapmaprs794729229
1000 genomesrs794729229
hgdprs794729229
ensemblrs794729229
gopubmedrs794729229
geneviewrs794729229
scholarrs794729229
googlers794729229
pharmgkbrs794729229
gwascentralrs794729229
openSNPrs794729229
23andMers794729229
23andMe allrs794729229
SNP Nexus

SNPshotrs794729229
SNPdbers794729229
MSV3drs794729229
GWAS Ctlgrs794729229
Max Magnitude0
ClinVar
Risk rs794729229(A;A)
Alt rs794729229(A;A)
Reference rs794729229(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome I
Variation info
Gene MSH2
CLNDBN Lynch syndrome I
Reversed 0
HGVS NC_000002.11:g.47707835G>A
CLNSRC
CLNACC RCV000184050.2,