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rs63750551

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
(I;I) 0
Make rs63750551(-;-)
Make rs63750551(-;AA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410257
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750551
ebirs63750551
HLIrs63750551
Exacrs63750551
Varsomers63750551
Maprs63750551
PheGenIrs63750551
hapmaprs63750551
1000 genomesrs63750551
hgdprs63750551
ensemblrs63750551
gopubmedrs63750551
geneviewrs63750551
scholarrs63750551
googlers63750551
pharmgkbrs63750551
gwascentralrs63750551
openSNPrs63750551
23andMers63750551
23andMe allrs63750551
SNP Nexus

SNPshotrs63750551
SNPdbers63750551
MSV3drs63750551
GWAS Ctlgrs63750551
Max Magnitude0
ClinVar
Risk rs63750551(;)
Alt rs63750551(;)
Reference rs63750551(AA;AA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637396_47637397delAA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076633.2,