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

rs63750516

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750516(-;-)
Make rs63750516(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429784
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750516
ebirs63750516
HLIrs63750516
Exacrs63750516
Varsomers63750516
Maprs63750516
PheGenIrs63750516
hapmaprs63750516
1000 genomesrs63750516
hgdprs63750516
ensemblrs63750516
gopubmedrs63750516
geneviewrs63750516
scholarrs63750516
googlers63750516
pharmgkbrs63750516
gwascentralrs63750516
openSNPrs63750516
23andMers63750516
23andMe allrs63750516
SNP Nexus

SNPshotrs63750516
SNPdbers63750516
MSV3drs63750516
GWAS Ctlgrs63750516
Max Magnitude0
ClinVar
Risk rs63750516(;)
Alt rs63750516(;)
Reference rs63750516(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47656923delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076042.2,