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rs587779065

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779065(A;A)
Make rs587779065(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47416366
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779065
dbSNP (old)rs587779065
ClinGenrs587779065
ebirs587779065
HLIrs587779065
Exacrs587779065
Gnomadrs587779065
Varsomers587779065
Maprs587779065
PheGenIrs587779065
Biobankrs587779065
1000 genomesrs587779065
hgdprs587779065
ensemblrs587779065
gopubmedrs587779065
geneviewrs587779065
scholarrs587779065
googlers587779065
pharmgkbrs587779065
gwascentralrs587779065
openSNPrs587779065
23andMers587779065
23andMe allrs587779065
SNP Nexus

SNPshotrs587779065
SNPdbers587779065
MSV3drs587779065
GWAS Ctlgrs587779065
Max Magnitude0
ClinVar
Risk rs587779065(A;A) rs587779065(C;C)
Alt rs587779065(A;A) rs587779065(C;C)
Reference Rs587779065(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47643505G>A; NC_000002.11:g.47643505G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075999.2, RCV000205553.1,