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

rs63750403

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750403(G;G)
Make rs63750403(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478292
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750403
ebirs63750403
HLIrs63750403
Exacrs63750403
Varsomers63750403
Maprs63750403
PheGenIrs63750403
hapmaprs63750403
1000 genomesrs63750403
hgdprs63750403
ensemblrs63750403
gopubmedrs63750403
geneviewrs63750403
scholarrs63750403
googlers63750403
pharmgkbrs63750403
gwascentralrs63750403
openSNPrs63750403
23andMers63750403
23andMe allrs63750403
SNP Nexus

SNPshotrs63750403
SNPdbers63750403
MSV3drs63750403
GWAS Ctlgrs63750403
Max Magnitude0
ClinVar
Risk rs63750403(G;G)
Alt rs63750403(G;G)
Reference rs63750403(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705431T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076437.2,