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

rs730880759

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880759(A;A)
Make rs730880759(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424068
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880759
ebirs730880759
HLIrs730880759
Exacrs730880759
Varsomers730880759
Maprs730880759
PheGenIrs730880759
hapmaprs730880759
1000 genomesrs730880759
hgdprs730880759
ensemblrs730880759
gopubmedrs730880759
geneviewrs730880759
scholarrs730880759
googlers730880759
pharmgkbrs730880759
gwascentralrs730880759
openSNPrs730880759
23andMers730880759
23andMe allrs730880759
SNP Nexus

SNPshotrs730880759
SNPdbers730880759
MSV3drs730880759
GWAS Ctlgrs730880759
Max Magnitude0
ClinVar
Risk rs730880759(A,T;A,T)
Alt rs730880759(A,T;A,T)
Reference rs730880759(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23893277C>T
CLNSRC
CLNACC RCV000158572.2,