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

rs730880675

From SNPedia

Orientationminus
Geno Mag Summary
(GTCTTTATCC;GTCTTTATCC) 0 common in clinvar
Make rs730880675(-;-)
Make rs730880675(-;GTCTTTATCC)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332823
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880675
ebirs730880675
HLIrs730880675
Exacrs730880675
Varsomers730880675
Maprs730880675
PheGenIrs730880675
hapmaprs730880675
1000 genomesrs730880675
hgdprs730880675
ensemblrs730880675
gopubmedrs730880675
geneviewrs730880675
scholarrs730880675
googlers730880675
pharmgkbrs730880675
gwascentralrs730880675
openSNPrs730880675
23andMers730880675
23andMe allrs730880675
SNP Nexus

SNPshotrs730880675
SNPdbers730880675
MSV3drs730880675
GWAS Ctlgrs730880675
Max Magnitude0
ClinVar
Risk rs730880675(;)
Alt rs730880675(;)
Reference rs730880675(GTCTTTATCC;GTCTTTATCC)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47354374_47354383delGGATAAAGAC
CLNSRC
CLNACC RCV000158403.1,