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

rs374946555

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs374946555(G;T)
Make rs374946555(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47335140
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs374946555
ebirs374946555
HLIrs374946555
Exacrs374946555
Varsomers374946555
Maprs374946555
PheGenIrs374946555
hapmaprs374946555
1000 genomesrs374946555
hgdprs374946555
ensemblrs374946555
gopubmedrs374946555
geneviewrs374946555
scholarrs374946555
googlers374946555
pharmgkbrs374946555
gwascentralrs374946555
openSNPrs374946555
23andMers374946555
23andMe allrs374946555
SNP Nexus

SNPshotrs374946555
SNPdbers374946555
MSV3drs374946555
GWAS Ctlgrs374946555
Max Magnitude0
ClinVar
Risk rs374946555(A,T;A,T)
Alt rs374946555(A,T;A,T)
Reference rs374946555(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene MYBPC3
CLNDBN not specified
Reversed 0
HGVS NC_000011.9:g.47356691G>A
CLNSRC
CLNACC RCV000158448.2,