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

rs730880654

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GCGCGTC;GCGCGTC) 0 common in clinvar
Make rs730880654(-;-)
Make rs730880654(-;GCGCGTC)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47337455
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880654
dbSNP (classic)rs730880654
ClinGenrs730880654
ebirs730880654
HLIrs730880654
Exacrs730880654
Gnomadrs730880654
Varsomers730880654
LitVarrs730880654
Maprs730880654
PheGenIrs730880654
Biobankrs730880654
1000 genomesrs730880654
hgdprs730880654
ensemblrs730880654
geneviewrs730880654
scholarrs730880654
googlers730880654
pharmgkbrs730880654
gwascentralrs730880654
openSNPrs730880654
23andMers730880654
SNPshotrs730880654
SNPdbers730880654
MSV3drs730880654
GWAS Ctlgrs730880654
Max Magnitude0
ClinVar
Risk rs730880654(-;-)
Alt rs730880654(-;-)
Reference Rs730880654(GCGCGTC;GCGCGTC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47359006_47359012delGACGCGC
CLNSRC
CLNACC RCV000158368.2,