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rs730880156

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880156(A;A)
Make rs730880156(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431868
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880156
ebirs730880156
HLIrs730880156
Exacrs730880156
Varsomers730880156
Maprs730880156
PheGenIrs730880156
hapmaprs730880156
1000 genomesrs730880156
hgdprs730880156
ensemblrs730880156
gopubmedrs730880156
geneviewrs730880156
scholarrs730880156
googlers730880156
pharmgkbrs730880156
gwascentralrs730880156
openSNPrs730880156
23andMers730880156
23andMe allrs730880156
SNP Nexus

SNPshotrs730880156
SNPdbers730880156
MSV3drs730880156
GWAS Ctlgrs730880156
Max Magnitude0
ClinVar
Risk rs730880156(A;A)
Alt rs730880156(A;A)
Reference rs730880156(G;G)
Significance Pathogenic
Disease Left ventricular noncompaction cardiomyopathy not provided
Variation info
Gene MYH7
CLNDBN Left ventricular noncompaction cardiomyopathy not provided
Reversed 1
HGVS NC_000014.8:g.23901077C>T
CLNSRC
CLNACC RCV000157350.1, RCV000225729.1,