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rs587779076

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs587779076(-;-)
Make rs587779076(-;CT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47429886
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779076
ebirs587779076
HLIrs587779076
Exacrs587779076
Varsomers587779076
Maprs587779076
PheGenIrs587779076
hapmaprs587779076
1000 genomesrs587779076
hgdprs587779076
ensemblrs587779076
gopubmedrs587779076
geneviewrs587779076
scholarrs587779076
googlers587779076
pharmgkbrs587779076
gwascentralrs587779076
openSNPrs587779076
23andMers587779076
23andMe allrs587779076
SNP Nexus

SNPshotrs587779076
SNPdbers587779076
MSV3drs587779076
GWAS Ctlgrs587779076
Max Magnitude0
ClinVar
Risk rs587779076(;)
Alt rs587779076(;)
Reference rs587779076(CT;CT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47657025_47657026delCT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076068.2,