Have questions? Visit https://www.reddit.com/r/SNPedia

rs63750210

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750210(-;-)
Make rs63750210(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410095
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750210
ebirs63750210
HLIrs63750210
Exacrs63750210
Varsomers63750210
Maprs63750210
PheGenIrs63750210
hapmaprs63750210
1000 genomesrs63750210
hgdprs63750210
ensemblrs63750210
gopubmedrs63750210
geneviewrs63750210
scholarrs63750210
googlers63750210
pharmgkbrs63750210
gwascentralrs63750210
openSNPrs63750210
23andMers63750210
23andMe allrs63750210
SNP Nexus

SNPshotrs63750210
SNPdbers63750210
MSV3drs63750210
GWAS Ctlgrs63750210
Max Magnitude0
ClinVar
Risk rs63750210(;)
Alt rs63750210(;)
Reference rs63750210(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637234delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076588.2,