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rs587782777

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782777(-;-)
Make rs587782777(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47429875
GeneMSH2
is asnp
is mentioned by
dbSNPrs587782777
ebirs587782777
HLIrs587782777
Exacrs587782777
Varsomers587782777
Maprs587782777
PheGenIrs587782777
hapmaprs587782777
1000 genomesrs587782777
hgdprs587782777
ensemblrs587782777
gopubmedrs587782777
geneviewrs587782777
scholarrs587782777
googlers587782777
pharmgkbrs587782777
gwascentralrs587782777
openSNPrs587782777
23andMers587782777
23andMe allrs587782777
SNP Nexus

SNPshotrs587782777
SNPdbers587782777
MSV3drs587782777
GWAS Ctlgrs587782777
Max Magnitude0
ClinVar
Risk rs587782777(;)
Alt rs587782777(;)
Reference rs587782777(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47657014delT
CLNSRC
CLNACC RCV000132311.2,