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rs587779108

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779108(A;A)
Make rs587779108(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47471063
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779108
ebirs587779108
HLIrs587779108
Exacrs587779108
Varsomers587779108
Maprs587779108
PheGenIrs587779108
hapmaprs587779108
1000 genomesrs587779108
hgdprs587779108
ensemblrs587779108
gopubmedrs587779108
geneviewrs587779108
scholarrs587779108
googlers587779108
pharmgkbrs587779108
gwascentralrs587779108
openSNPrs587779108
23andMers587779108
23andMe allrs587779108
SNP Nexus

SNPshotrs587779108
SNPdbers587779108
MSV3drs587779108
GWAS Ctlgrs587779108
Max Magnitude0
ClinVar
Risk rs587779108(A;A)
Alt rs587779108(A;A)
Reference rs587779108(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH2
CLNDBN Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.47698202G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076265.2, RCV000213952.1,