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rs63750910

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750910(C;G)
Make rs63750910(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410152
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750910
ebirs63750910
HLIrs63750910
Exacrs63750910
Varsomers63750910
Maprs63750910
PheGenIrs63750910
hapmaprs63750910
1000 genomesrs63750910
hgdprs63750910
ensemblrs63750910
gopubmedrs63750910
geneviewrs63750910
scholarrs63750910
googlers63750910
pharmgkbrs63750910
gwascentralrs63750910
openSNPrs63750910
23andMers63750910
23andMe allrs63750910
SNP Nexus

SNPshotrs63750910
SNPdbers63750910
MSV3drs63750910
GWAS Ctlgrs63750910
Max Magnitude0
ClinVar
Risk rs63750910(G;G)
Alt rs63750910(G;G)
Reference rs63750910(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637291C>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076598.2,