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rs63751403

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751403(C;T)
Make rs63751403(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47463062
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751403
ebirs63751403
HLIrs63751403
Exacrs63751403
Varsomers63751403
Maprs63751403
PheGenIrs63751403
hapmaprs63751403
1000 genomesrs63751403
hgdprs63751403
ensemblrs63751403
gopubmedrs63751403
geneviewrs63751403
scholarrs63751403
googlers63751403
pharmgkbrs63751403
gwascentralrs63751403
openSNPrs63751403
23andMers63751403
23andMe allrs63751403
SNP Nexus

SNPshotrs63751403
SNPdbers63751403
MSV3drs63751403
GWAS Ctlgrs63751403
Max Magnitude0
ClinVar
Risk rs63751403(G,T;G,T)
Alt rs63751403(G,T;G,T)
Reference rs63751403(C;C)
Significance Pathogenic
Disease Lynch syndrome Colorectal cancer Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH2
CLNDBN Lynch syndrome Colorectal cancer, non-polyposis Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.47690201C>G; NC_000002.11:g.47690201C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076155.2, RCV000076156.2, RCV000148630.1, RCV000218562.1,