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rs63750267

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750267(C;T)
Make rs63750267(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429794
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750267
ebirs63750267
HLIrs63750267
Exacrs63750267
Varsomers63750267
Maprs63750267
PheGenIrs63750267
hapmaprs63750267
1000 genomesrs63750267
hgdprs63750267
ensemblrs63750267
gopubmedrs63750267
geneviewrs63750267
scholarrs63750267
googlers63750267
pharmgkbrs63750267
gwascentralrs63750267
openSNPrs63750267
23andMers63750267
23andMe allrs63750267
SNP Nexus

SNPshotrs63750267
SNPdbers63750267
MSV3drs63750267
GWAS Ctlgrs63750267
Max Magnitude0
ClinVar
Risk rs63750267(G,T;G,T)
Alt rs63750267(G,T;G,T)
Reference rs63750267(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47656933C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076045.2,