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rs587779094

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779094(-;-)
Make rs587779094(-;C)
Make rs587779094(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47463144
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779094
ebirs587779094
HLIrs587779094
Exacrs587779094
Varsomers587779094
Maprs587779094
PheGenIrs587779094
hapmaprs587779094
1000 genomesrs587779094
hgdprs587779094
ensemblrs587779094
gopubmedrs587779094
geneviewrs587779094
scholarrs587779094
googlers587779094
pharmgkbrs587779094
gwascentralrs587779094
openSNPrs587779094
23andMers587779094
23andMe allrs587779094
SNP Nexus

SNPshotrs587779094
SNPdbers587779094
MSV3drs587779094
GWAS Ctlgrs587779094
Max Magnitude0
ClinVar
Risk rs587779094(C;C)
Alt rs587779094(C;C)
Reference rs587779094(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690283dupC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076179.2,