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rs587779117

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs587779117(-;-)
Make rs587779117(-;GT)
Make rs587779117(GT;GT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47475189
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779117
ebirs587779117
HLIrs587779117
Exacrs587779117
Varsomers587779117
Maprs587779117
PheGenIrs587779117
hapmaprs587779117
1000 genomesrs587779117
hgdprs587779117
ensemblrs587779117
gopubmedrs587779117
geneviewrs587779117
scholarrs587779117
googlers587779117
pharmgkbrs587779117
gwascentralrs587779117
openSNPrs587779117
23andMers587779117
23andMe allrs587779117
SNP Nexus

SNPshotrs587779117
SNPdbers587779117
MSV3drs587779117
GWAS Ctlgrs587779117
Max Magnitude0
ClinVar
Risk rs587779117(;)
Alt rs587779117(;)
Reference rs587779117(TG;TG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702328_47702329delGT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076323.2,