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rs587779124

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779124(-;-)
Make rs587779124(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47475272
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779124
ebirs587779124
HLIrs587779124
Exacrs587779124
Varsomers587779124
Maprs587779124
PheGenIrs587779124
hapmaprs587779124
1000 genomesrs587779124
hgdprs587779124
ensemblrs587779124
gopubmedrs587779124
geneviewrs587779124
scholarrs587779124
googlers587779124
pharmgkbrs587779124
gwascentralrs587779124
openSNPrs587779124
23andMers587779124
23andMe allrs587779124
SNP Nexus

SNPshotrs587779124
SNPdbers587779124
MSV3drs587779124
GWAS Ctlgrs587779124
Max Magnitude0
ClinVar
Risk rs587779124(;)
Alt rs587779124(;)
Reference rs587779124(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702411delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076343.2,