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rs63750382

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750382(G;T)
Make rs63750382(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410256
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750382
ebirs63750382
HLIrs63750382
Exacrs63750382
Varsomers63750382
Maprs63750382
PheGenIrs63750382
hapmaprs63750382
1000 genomesrs63750382
hgdprs63750382
ensemblrs63750382
gopubmedrs63750382
geneviewrs63750382
scholarrs63750382
googlers63750382
pharmgkbrs63750382
gwascentralrs63750382
openSNPrs63750382
23andMers63750382
23andMe allrs63750382
SNP Nexus

SNPshotrs63750382
SNPdbers63750382
MSV3drs63750382
GWAS Ctlgrs63750382
Max Magnitude0
ClinVar
Risk rs63750382(A,T;A,T)
Alt rs63750382(A,T;A,T)
Reference rs63750382(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637395G>A; NC_000002.11:g.47637395G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076631.2, RCV000076632.2,