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rs63749854

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63749854(G;T)
Make rs63749854(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478336
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749854
ebirs63749854
HLIrs63749854
Exacrs63749854
Varsomers63749854
Maprs63749854
PheGenIrs63749854
hapmaprs63749854
1000 genomesrs63749854
hgdprs63749854
ensemblrs63749854
gopubmedrs63749854
geneviewrs63749854
scholarrs63749854
googlers63749854
pharmgkbrs63749854
gwascentralrs63749854
openSNPrs63749854
23andMers63749854
23andMe allrs63749854
SNP Nexus

SNPshotrs63749854
SNPdbers63749854
MSV3drs63749854
GWAS Ctlgrs63749854
Max Magnitude0
ClinVar
Risk rs63749854(T;T)
Alt rs63749854(T;T)
Reference rs63749854(G;G)
Significance Pathogenic
Disease Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH2
CLNDBN Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.47705475G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076448.2, RCV000223378.1,