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rs587779112

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779112(-;-)
Make rs587779112(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47475092
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779112
ClinGenrs587779112
ebirs587779112
HLIrs587779112
Exacrs587779112
Varsomers587779112
Maprs587779112
PheGenIrs587779112
hapmaprs587779112
1000 genomesrs587779112
hgdprs587779112
ensemblrs587779112
gopubmedrs587779112
geneviewrs587779112
scholarrs587779112
googlers587779112
pharmgkbrs587779112
gwascentralrs587779112
openSNPrs587779112
23andMers587779112
23andMe allrs587779112
SNP Nexus

SNPshotrs587779112
SNPdbers587779112
MSV3drs587779112
GWAS Ctlgrs587779112
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs587779112(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702231delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076297.2,