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rs63750496

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63750496(-;-)
Make rs63750496(-;C)
Make rs63750496(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429809
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750496
ebirs63750496
HLIrs63750496
Exacrs63750496
Varsomers63750496
Maprs63750496
PheGenIrs63750496
hapmaprs63750496
1000 genomesrs63750496
hgdprs63750496
ensemblrs63750496
gopubmedrs63750496
geneviewrs63750496
scholarrs63750496
googlers63750496
pharmgkbrs63750496
gwascentralrs63750496
openSNPrs63750496
23andMers63750496
23andMe allrs63750496
SNP Nexus

SNPshotrs63750496
SNPdbers63750496
MSV3drs63750496
GWAS Ctlgrs63750496
Max Magnitude0
ClinVar
Risk rs63750496(C;C)
Alt rs63750496(C;C)
Reference rs63750496(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47656948dupC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076047.2,