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rs730880901

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880901(A;T)
Make rs730880901(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23423971
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880901
ebirs730880901
HLIrs730880901
Exacrs730880901
Varsomers730880901
Maprs730880901
PheGenIrs730880901
hapmaprs730880901
1000 genomesrs730880901
hgdprs730880901
ensemblrs730880901
gopubmedrs730880901
geneviewrs730880901
scholarrs730880901
googlers730880901
pharmgkbrs730880901
gwascentralrs730880901
openSNPrs730880901
23andMers730880901
23andMe allrs730880901
SNP Nexus

SNPshotrs730880901
SNPdbers730880901
MSV3drs730880901
GWAS Ctlgrs730880901
Max Magnitude0
ClinVar
Risk rs730880901(T;T)
Alt rs730880901(T;T)
Reference rs730880901(A;A)
Significance Pathogenic
Disease not provided not specified Hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN not provided not specified Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23893180T>A
CLNSRC
CLNACC RCV000158855.1, RCV000223789.1, RCV000226190.1,