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rs587779121

From SNPedia

Orientationplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs587779121(-;-)
Make rs587779121(-;CA)
Make rs587779121(CA;CA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47475249
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779121
ebirs587779121
HLIrs587779121
Exacrs587779121
Varsomers587779121
Maprs587779121
PheGenIrs587779121
hapmaprs587779121
1000 genomesrs587779121
hgdprs587779121
ensemblrs587779121
gopubmedrs587779121
geneviewrs587779121
scholarrs587779121
googlers587779121
pharmgkbrs587779121
gwascentralrs587779121
openSNPrs587779121
23andMers587779121
23andMe allrs587779121
SNP Nexus

SNPshotrs587779121
SNPdbers587779121
MSV3drs587779121
GWAS Ctlgrs587779121
Max Magnitude0
ClinVar
Risk rs587779121(;)
Alt rs587779121(;)
Reference rs587779121(AC;AC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702388_47702389delCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076330.2,