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rs730880916

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880916(A;A)
Make rs730880916(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415410
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880916
ebirs730880916
HLIrs730880916
Exacrs730880916
Varsomers730880916
Maprs730880916
PheGenIrs730880916
hapmaprs730880916
1000 genomesrs730880916
hgdprs730880916
ensemblrs730880916
gopubmedrs730880916
geneviewrs730880916
scholarrs730880916
googlers730880916
pharmgkbrs730880916
gwascentralrs730880916
openSNPrs730880916
23andMers730880916
23andMe allrs730880916
SNP Nexus

SNPshotrs730880916
SNPdbers730880916
MSV3drs730880916
GWAS Ctlgrs730880916
Max Magnitude0
ClinVar
Risk rs730880916(A;A)
Alt rs730880916(A;A)
Reference rs730880916(G;G)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7 MHRT
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23884619C>T
CLNSRC
CLNACC RCV000158871.1,