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rs587779138

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779138(G;G)
Make rs587779138(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47407923
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779138
ebirs587779138
HLIrs587779138
Exacrs587779138
Varsomers587779138
Maprs587779138
PheGenIrs587779138
hapmaprs587779138
1000 genomesrs587779138
hgdprs587779138
ensemblrs587779138
gopubmedrs587779138
geneviewrs587779138
scholarrs587779138
googlers587779138
pharmgkbrs587779138
gwascentralrs587779138
openSNPrs587779138
23andMers587779138
23andMe allrs587779138
SNP Nexus

SNPshotrs587779138
SNPdbers587779138
MSV3drs587779138
GWAS Ctlgrs587779138
Max Magnitude0
ClinVar
Risk rs587779138(G;G)
Alt rs587779138(G;G)
Reference rs587779138(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47635062T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076396.2,