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rs587779091

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779091(-;-)
Make rs587779091(-;TC)
Make rs587779091(TC;TC)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47463078
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779091
ebirs587779091
HLIrs587779091
Exacrs587779091
Varsomers587779091
Maprs587779091
PheGenIrs587779091
hapmaprs587779091
1000 genomesrs587779091
hgdprs587779091
ensemblrs587779091
gopubmedrs587779091
geneviewrs587779091
scholarrs587779091
googlers587779091
pharmgkbrs587779091
gwascentralrs587779091
openSNPrs587779091
23andMers587779091
23andMe allrs587779091
SNP Nexus

SNPshotrs587779091
SNPdbers587779091
MSV3drs587779091
GWAS Ctlgrs587779091
Max Magnitude0
ClinVar
Risk rs587779091(TC;TC)
Alt rs587779091(TC;TC)
Reference rs587779091(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690216_47690217dupTC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076159.2,