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rs63750203

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750203(C;T)
Make rs63750203(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475150
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750203
ebirs63750203
HLIrs63750203
Exacrs63750203
Varsomers63750203
Maprs63750203
PheGenIrs63750203
hapmaprs63750203
1000 genomesrs63750203
hgdprs63750203
ensemblrs63750203
gopubmedrs63750203
geneviewrs63750203
scholarrs63750203
googlers63750203
pharmgkbrs63750203
gwascentralrs63750203
openSNPrs63750203
23andMers63750203
23andMe allrs63750203
SNP Nexus

SNPshotrs63750203
SNPdbers63750203
MSV3drs63750203
GWAS Ctlgrs63750203
Max Magnitude0
ClinVar
Risk rs63750203(T;T)
Alt rs63750203(T;T)
Reference rs63750203(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702289C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076313.2,