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rs63749802

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63749802(G;T)
Make rs63749802(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47476552
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749802
ebirs63749802
HLIrs63749802
Exacrs63749802
Varsomers63749802
Maprs63749802
PheGenIrs63749802
hapmaprs63749802
1000 genomesrs63749802
hgdprs63749802
ensemblrs63749802
gopubmedrs63749802
geneviewrs63749802
scholarrs63749802
googlers63749802
pharmgkbrs63749802
gwascentralrs63749802
openSNPrs63749802
23andMers63749802
23andMe allrs63749802
SNP Nexus

SNPshotrs63749802
SNPdbers63749802
MSV3drs63749802
GWAS Ctlgrs63749802
Max Magnitude0
ClinVar
Risk rs63749802(T;T)
Alt rs63749802(T;T)
Reference rs63749802(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703691G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076417.2,