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

rs63749902

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63749902(-;-)
Make rs63749902(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47414271
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749902
ebirs63749902
HLIrs63749902
Exacrs63749902
Varsomers63749902
Maprs63749902
PheGenIrs63749902
hapmaprs63749902
1000 genomesrs63749902
hgdprs63749902
ensemblrs63749902
gopubmedrs63749902
geneviewrs63749902
scholarrs63749902
googlers63749902
pharmgkbrs63749902
gwascentralrs63749902
openSNPrs63749902
23andMers63749902
23andMe allrs63749902
SNP Nexus

SNPshotrs63749902
SNPdbers63749902
MSV3drs63749902
GWAS Ctlgrs63749902
Max Magnitude0
ClinVar
Risk rs63749902(;)
Alt rs63749902(;)
Reference rs63749902(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641410delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076723.2,