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rs63750615

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750615(G;T)
Make rs63750615(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47403333
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750615
ebirs63750615
HLIrs63750615
Exacrs63750615
Varsomers63750615
Maprs63750615
PheGenIrs63750615
hapmaprs63750615
1000 genomesrs63750615
hgdprs63750615
ensemblrs63750615
gopubmedrs63750615
geneviewrs63750615
scholarrs63750615
googlers63750615
pharmgkbrs63750615
gwascentralrs63750615
openSNPrs63750615
23andMers63750615
23andMe allrs63750615
SNP Nexus

SNPshotrs63750615
SNPdbers63750615
MSV3drs63750615
GWAS Ctlgrs63750615
Max Magnitude0
ClinVar
Risk rs63750615(T;T)
Alt rs63750615(T;T)
Reference rs63750615(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47630472G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076158.2,