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rs587779083

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs587779083(-;-)
Make rs587779083(-;CT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47445589
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779083
ebirs587779083
HLIrs587779083
Exacrs587779083
Varsomers587779083
Maprs587779083
PheGenIrs587779083
hapmaprs587779083
1000 genomesrs587779083
hgdprs587779083
ensemblrs587779083
gopubmedrs587779083
geneviewrs587779083
scholarrs587779083
googlers587779083
pharmgkbrs587779083
gwascentralrs587779083
openSNPrs587779083
23andMers587779083
23andMe allrs587779083
SNP Nexus

SNPshotrs587779083
SNPdbers587779083
MSV3drs587779083
GWAS Ctlgrs587779083
Max Magnitude0
ClinVar
Risk rs587779083(;)
Alt rs587779083(;)
Reference rs587779083(CT;CT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47672728_47672729delCT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076120.2,