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rs587779195

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779195(G;G)
Make rs587779195(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47414420
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779195
ebirs587779195
HLIrs587779195
Exacrs587779195
Varsomers587779195
Maprs587779195
PheGenIrs587779195
hapmaprs587779195
1000 genomesrs587779195
hgdprs587779195
ensemblrs587779195
gopubmedrs587779195
geneviewrs587779195
scholarrs587779195
googlers587779195
pharmgkbrs587779195
gwascentralrs587779195
openSNPrs587779195
23andMers587779195
23andMe allrs587779195
SNP Nexus

SNPshotrs587779195
SNPdbers587779195
MSV3drs587779195
GWAS Ctlgrs587779195
Max Magnitude0
ClinVar
Risk rs587779195(C,G;C,G)
Alt rs587779195(C,G;C,G)
Reference rs587779195(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641559T>C; NC_000002.11:g.47641559T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000132128.2, RCV000076754.2,