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rs587779166

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779166(A;A)
Make rs587779166(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47410319
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779166
ebirs587779166
HLIrs587779166
Exacrs587779166
Varsomers587779166
Maprs587779166
PheGenIrs587779166
hapmaprs587779166
1000 genomesrs587779166
hgdprs587779166
ensemblrs587779166
gopubmedrs587779166
geneviewrs587779166
scholarrs587779166
googlers587779166
pharmgkbrs587779166
gwascentralrs587779166
openSNPrs587779166
23andMers587779166
23andMe allrs587779166
SNP Nexus

SNPshotrs587779166
SNPdbers587779166
MSV3drs587779166
GWAS Ctlgrs587779166
Max Magnitude0
ClinVar
Risk rs587779166(A,T;A,T)
Alt rs587779166(A,T;A,T)
Reference rs587779166(G;G)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47637458G>A; NC_000002.11:g.47637458G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076647.2, RCV000160618.1,