Have questions? Visit https://www.reddit.com/r/SNPedia

rs587779165

From SNPedia

Orientationplus
Geno Mag Summary
(CTC;CTC) 0 common in clinvar
Make rs587779165(-;-)
Make rs587779165(-;CTC)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47410298
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779165
ebirs587779165
HLIrs587779165
Exacrs587779165
Varsomers587779165
Maprs587779165
PheGenIrs587779165
hapmaprs587779165
1000 genomesrs587779165
hgdprs587779165
ensemblrs587779165
gopubmedrs587779165
geneviewrs587779165
scholarrs587779165
googlers587779165
pharmgkbrs587779165
gwascentralrs587779165
openSNPrs587779165
23andMers587779165
23andMe allrs587779165
SNP Nexus

SNPshotrs587779165
SNPdbers587779165
MSV3drs587779165
GWAS Ctlgrs587779165
Max Magnitude0
ClinVar
Risk rs587779165(;)
Alt rs587779165(;)
Reference rs587779165(CTC;CTC)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47637437_47637439delCTC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076643.2, RCV000160632.1,