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rs63750463

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750463(-;-)
Make rs63750463(-;A)
Make rs63750463(A;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478423
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750463
ebirs63750463
HLIrs63750463
Exacrs63750463
Varsomers63750463
Maprs63750463
PheGenIrs63750463
hapmaprs63750463
1000 genomesrs63750463
hgdprs63750463
ensemblrs63750463
gopubmedrs63750463
geneviewrs63750463
scholarrs63750463
googlers63750463
pharmgkbrs63750463
gwascentralrs63750463
openSNPrs63750463
23andMers63750463
23andMe allrs63750463
SNP Nexus

SNPshotrs63750463
SNPdbers63750463
MSV3drs63750463
GWAS Ctlgrs63750463
Max Magnitude0
ClinVar
Risk rs63750463(A;A)
Alt rs63750463(A;A)
Reference rs63750463(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705562dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076464.2,