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rs587779088

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779088(-;-)
Make rs587779088(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47463034
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779088
ebirs587779088
HLIrs587779088
Exacrs587779088
Varsomers587779088
Maprs587779088
PheGenIrs587779088
hapmaprs587779088
1000 genomesrs587779088
hgdprs587779088
ensemblrs587779088
gopubmedrs587779088
geneviewrs587779088
scholarrs587779088
googlers587779088
pharmgkbrs587779088
gwascentralrs587779088
openSNPrs587779088
23andMers587779088
23andMe allrs587779088
SNP Nexus

SNPshotrs587779088
SNPdbers587779088
MSV3drs587779088
GWAS Ctlgrs587779088
Max Magnitude0
ClinVar
Risk rs587779088(;)
Alt rs587779088(;)
Reference rs587779088(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690173delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076151.2,