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rs587779197

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779197(A;A)
Make rs587779197(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47414418
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779197
ebirs587779197
HLIrs587779197
Exacrs587779197
Varsomers587779197
Maprs587779197
PheGenIrs587779197
hapmaprs587779197
1000 genomesrs587779197
hgdprs587779197
ensemblrs587779197
gopubmedrs587779197
geneviewrs587779197
scholarrs587779197
googlers587779197
pharmgkbrs587779197
gwascentralrs587779197
openSNPrs587779197
23andMers587779197
23andMe allrs587779197
SNP Nexus

SNPshotrs587779197
SNPdbers587779197
MSV3drs587779197
GWAS Ctlgrs587779197
Max Magnitude0
ClinVar
Risk rs587779197(A;A)
Alt rs587779197(A;A)
Reference rs587779197(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641557G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076756.2,