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rs587779089

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779089(G;T)
Make rs587779089(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47463043
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779089
ebirs587779089
HLIrs587779089
Exacrs587779089
Varsomers587779089
Maprs587779089
PheGenIrs587779089
hapmaprs587779089
1000 genomesrs587779089
hgdprs587779089
ensemblrs587779089
gopubmedrs587779089
geneviewrs587779089
scholarrs587779089
googlers587779089
pharmgkbrs587779089
gwascentralrs587779089
openSNPrs587779089
23andMers587779089
23andMe allrs587779089
SNP Nexus

SNPshotrs587779089
SNPdbers587779089
MSV3drs587779089
GWAS Ctlgrs587779089
Max Magnitude0
ClinVar
Risk rs587779089(T;T)
Alt rs587779089(T;T)
Reference rs587779089(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690182G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076152.2,