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

rs63749832

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs63749832(-;-)
Make rs63749832(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47412514
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749832
ebirs63749832
HLIrs63749832
Exacrs63749832
Varsomers63749832
Maprs63749832
PheGenIrs63749832
hapmaprs63749832
1000 genomesrs63749832
hgdprs63749832
ensemblrs63749832
gopubmedrs63749832
geneviewrs63749832
scholarrs63749832
googlers63749832
pharmgkbrs63749832
gwascentralrs63749832
openSNPrs63749832
23andMers63749832
23andMe allrs63749832
SNP Nexus

SNPshotrs63749832
SNPdbers63749832
MSV3drs63749832
GWAS Ctlgrs63749832
Max Magnitude0
ClinVar
Risk rs63749832(;)
Alt rs63749832(;)
Reference rs63749832(A;A)
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.47639653delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076699.2, RCV000164791.1,