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

rs63749915

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63749915(A;T)
Make rs63749915(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47414377
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749915
ebirs63749915
HLIrs63749915
Exacrs63749915
Varsomers63749915
Maprs63749915
PheGenIrs63749915
hapmaprs63749915
1000 genomesrs63749915
hgdprs63749915
ensemblrs63749915
gopubmedrs63749915
geneviewrs63749915
scholarrs63749915
googlers63749915
pharmgkbrs63749915
gwascentralrs63749915
openSNPrs63749915
23andMers63749915
23andMe allrs63749915
SNP Nexus

SNPshotrs63749915
SNPdbers63749915
MSV3drs63749915
GWAS Ctlgrs63749915
Max Magnitude0
ClinVar
Risk rs63749915(T;T)
Alt rs63749915(T;T)
Reference rs63749915(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641516A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076746.2,