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rs587779192

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779192(-;-)
Make rs587779192(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47414364
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779192
ebirs587779192
HLIrs587779192
Exacrs587779192
Varsomers587779192
Maprs587779192
PheGenIrs587779192
hapmaprs587779192
1000 genomesrs587779192
hgdprs587779192
ensemblrs587779192
gopubmedrs587779192
geneviewrs587779192
scholarrs587779192
googlers587779192
pharmgkbrs587779192
gwascentralrs587779192
openSNPrs587779192
23andMers587779192
23andMe allrs587779192
SNP Nexus

SNPshotrs587779192
SNPdbers587779192
MSV3drs587779192
GWAS Ctlgrs587779192
Max Magnitude0
ClinVar
Risk rs587779192(;)
Alt rs587779192(;)
Reference rs587779192(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641503delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076743.2,