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rs587779170

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779170(C;T)
Make rs587779170(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47412420
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779170
ebirs587779170
HLIrs587779170
Exacrs587779170
Varsomers587779170
Maprs587779170
PheGenIrs587779170
hapmaprs587779170
1000 genomesrs587779170
hgdprs587779170
ensemblrs587779170
gopubmedrs587779170
geneviewrs587779170
scholarrs587779170
googlers587779170
pharmgkbrs587779170
gwascentralrs587779170
openSNPrs587779170
23andMers587779170
23andMe allrs587779170
SNP Nexus

SNPshotrs587779170
SNPdbers587779170
MSV3drs587779170
GWAS Ctlgrs587779170
Max Magnitude0
ClinVar
Risk rs587779170(T;T)
Alt rs587779170(T;T)
Reference rs587779170(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639559C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076677.2,