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rs63750039

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0
(T;T) 0 common in clinvar
Make rs63750039(-;-)
Make rs63750039(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429804
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750039
ebirs63750039
HLIrs63750039
Exacrs63750039
Varsomers63750039
Maprs63750039
PheGenIrs63750039
hapmaprs63750039
1000 genomesrs63750039
hgdprs63750039
ensemblrs63750039
gopubmedrs63750039
geneviewrs63750039
scholarrs63750039
googlers63750039
pharmgkbrs63750039
gwascentralrs63750039
openSNPrs63750039
23andMers63750039
23andMe allrs63750039
SNP Nexus

SNPshotrs63750039
SNPdbers63750039
MSV3drs63750039
GWAS Ctlgrs63750039
Max Magnitude0
ClinVar
Risk rs63750039(;)
Alt rs63750039(;)
Reference rs63750039(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47656943delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076046.2,