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rs63750233

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(I;I) 0
Make rs63750233(-;-)
Make rs63750233(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478408
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750233
ebirs63750233
HLIrs63750233
Exacrs63750233
Varsomers63750233
Maprs63750233
PheGenIrs63750233
hapmaprs63750233
1000 genomesrs63750233
hgdprs63750233
ensemblrs63750233
gopubmedrs63750233
geneviewrs63750233
scholarrs63750233
googlers63750233
pharmgkbrs63750233
gwascentralrs63750233
openSNPrs63750233
23andMers63750233
23andMe allrs63750233
SNP Nexus

SNPshotrs63750233
SNPdbers63750233
MSV3drs63750233
GWAS Ctlgrs63750233
Max Magnitude0
ClinVar
Risk rs63750233(;)
Alt rs63750233(;)
Reference rs63750233(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705547delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076461.2,