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

rs200399246

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200399246(A;A)
Make rs200399246(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47338658
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs200399246
ebirs200399246
HLIrs200399246
Exacrs200399246
Varsomers200399246
Maprs200399246
PheGenIrs200399246
hapmaprs200399246
1000 genomesrs200399246
hgdprs200399246
ensemblrs200399246
gopubmedrs200399246
geneviewrs200399246
scholarrs200399246
googlers200399246
pharmgkbrs200399246
gwascentralrs200399246
openSNPrs200399246
23andMers200399246
23andMe allrs200399246
SNP Nexus

SNPshotrs200399246
SNPdbers200399246
MSV3drs200399246
GWAS Ctlgrs200399246
Max Magnitude0
ClinVar
Risk rs200399246(A;A)
Alt rs200399246(A;A)
Reference rs200399246(G;G)
Significance Probable-Pathogenic
Disease not specified not provided Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN not specified not provided Familial hypertrophic cardiomyopathy 4
Reversed 0
HGVS NC_000011.9:g.47360209G>A
CLNSRC
CLNACC RCV000154554.2, RCV000158139.1, RCV000168793.1,