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rs63750008

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0
(T;T) 0 common in clinvar
Make rs63750008(-;-)
Make rs63750008(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47480744
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750008
ebirs63750008
HLIrs63750008
Exacrs63750008
Varsomers63750008
Maprs63750008
PheGenIrs63750008
hapmaprs63750008
1000 genomesrs63750008
hgdprs63750008
ensemblrs63750008
gopubmedrs63750008
geneviewrs63750008
scholarrs63750008
googlers63750008
pharmgkbrs63750008
gwascentralrs63750008
openSNPrs63750008
23andMers63750008
23andMe allrs63750008
SNP Nexus

SNPshotrs63750008
SNPdbers63750008
MSV3drs63750008
GWAS Ctlgrs63750008
Max Magnitude0
ClinVar
Risk rs63750008(;)
Alt rs63750008(;)
Reference rs63750008(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47707883delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076491.2,