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rs587779183

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779183(C;C)
Make rs587779183(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47412560
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779183
ebirs587779183
HLIrs587779183
Exacrs587779183
Varsomers587779183
Maprs587779183
PheGenIrs587779183
hapmaprs587779183
1000 genomesrs587779183
hgdprs587779183
ensemblrs587779183
gopubmedrs587779183
geneviewrs587779183
scholarrs587779183
googlers587779183
pharmgkbrs587779183
gwascentralrs587779183
openSNPrs587779183
23andMers587779183
23andMe allrs587779183
SNP Nexus

SNPshotrs587779183
SNPdbers587779183
MSV3drs587779183
GWAS Ctlgrs587779183
Max Magnitude0
ClinVar
Risk rs587779183(A,C;A,C)
Alt rs587779183(A,C;A,C)
Reference rs587779183(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639699G>A; NC_000002.11:g.47639699G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000228778.1, RCV000076712.2,