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

rs730880607

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880607(A;T)
Make rs730880607(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332092
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880607
ebirs730880607
HLIrs730880607
Exacrs730880607
Varsomers730880607
Maprs730880607
PheGenIrs730880607
hapmaprs730880607
1000 genomesrs730880607
hgdprs730880607
ensemblrs730880607
gopubmedrs730880607
geneviewrs730880607
scholarrs730880607
googlers730880607
pharmgkbrs730880607
gwascentralrs730880607
openSNPrs730880607
23andMers730880607
23andMe allrs730880607
SNP Nexus

SNPshotrs730880607
SNPdbers730880607
MSV3drs730880607
GWAS Ctlgrs730880607
Max Magnitude0
ClinVar
Risk rs730880607(T;T)
Alt rs730880607(T;T)
Reference rs730880607(A;A)
Significance Pathogenic
Disease not specified
Variation info
Gene MYBPC3
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.47353643T>A
CLNSRC
CLNACC RCV000158268.2,