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rs587779110

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779110(A;A)
Make rs587779110(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47475024
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779110
ebirs587779110
HLIrs587779110
Exacrs587779110
Varsomers587779110
Maprs587779110
PheGenIrs587779110
hapmaprs587779110
1000 genomesrs587779110
hgdprs587779110
ensemblrs587779110
gopubmedrs587779110
geneviewrs587779110
scholarrs587779110
googlers587779110
pharmgkbrs587779110
gwascentralrs587779110
openSNPrs587779110
23andMers587779110
23andMe allrs587779110
SNP Nexus

SNPshotrs587779110
SNPdbers587779110
MSV3drs587779110
GWAS Ctlgrs587779110
Max Magnitude0
ClinVar
Risk rs587779110(A;A)
Alt rs587779110(A;A)
Reference rs587779110(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702163G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076272.2,