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

rs63750564

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750564(A;A)
Make rs63750564(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47799818
GeneMSH6
is asnp
is mentioned by
dbSNPrs63750564
ebirs63750564
HLIrs63750564
Exacrs63750564
Varsomers63750564
Maprs63750564
PheGenIrs63750564
hapmaprs63750564
1000 genomesrs63750564
hgdprs63750564
ensemblrs63750564
gopubmedrs63750564
geneviewrs63750564
scholarrs63750564
googlers63750564
pharmgkbrs63750564
gwascentralrs63750564
openSNPrs63750564
23andMers63750564
23andMe allrs63750564
SNP Nexus

SNPshotrs63750564
SNPdbers63750564
MSV3drs63750564
GWAS Ctlgrs63750564
Max Magnitude0
ClinVar
Risk rs63750564(A;A)
Alt rs63750564(A;A)
Reference rs63750564(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026957C>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074690.2,