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rs730880909

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880909(C;G)
Make rs730880909(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23418238
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880909
ebirs730880909
HLIrs730880909
Exacrs730880909
Varsomers730880909
Maprs730880909
PheGenIrs730880909
hapmaprs730880909
1000 genomesrs730880909
hgdprs730880909
ensemblrs730880909
gopubmedrs730880909
geneviewrs730880909
scholarrs730880909
googlers730880909
pharmgkbrs730880909
gwascentralrs730880909
openSNPrs730880909
23andMers730880909
23andMe allrs730880909
SNP Nexus

SNPshotrs730880909
SNPdbers730880909
MSV3drs730880909
GWAS Ctlgrs730880909
Max Magnitude0
ClinVar
Risk rs730880909(G;G)
Alt rs730880909(G;G)
Reference rs730880909(C;C)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7 MIR208B
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23887447G>C
CLNSRC
CLNACC RCV000158863.1,