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rs63750545

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63750545(-;-)
Make rs63750545(-;C)
Make rs63750545(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47476502
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750545
ebirs63750545
HLIrs63750545
Exacrs63750545
Varsomers63750545
Maprs63750545
PheGenIrs63750545
hapmaprs63750545
1000 genomesrs63750545
hgdprs63750545
ensemblrs63750545
gopubmedrs63750545
geneviewrs63750545
scholarrs63750545
googlers63750545
pharmgkbrs63750545
gwascentralrs63750545
openSNPrs63750545
23andMers63750545
23andMe allrs63750545
SNP Nexus

SNPshotrs63750545
SNPdbers63750545
MSV3drs63750545
GWAS Ctlgrs63750545
Max Magnitude0
ClinVar
Risk rs63750545(C;C)
Alt rs63750545(C;C)
Reference rs63750545(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703641dupC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076410.2,