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rs730880729

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880729(A;A)
Make rs730880729(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23432768
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880729
ebirs730880729
HLIrs730880729
Exacrs730880729
Varsomers730880729
Maprs730880729
PheGenIrs730880729
hapmaprs730880729
1000 genomesrs730880729
hgdprs730880729
ensemblrs730880729
gopubmedrs730880729
geneviewrs730880729
scholarrs730880729
googlers730880729
pharmgkbrs730880729
gwascentralrs730880729
openSNPrs730880729
23andMers730880729
23andMe allrs730880729
SNP Nexus

SNPshotrs730880729
SNPdbers730880729
MSV3drs730880729
GWAS Ctlgrs730880729
Max Magnitude0
ClinVar
Risk rs730880729(A,T;A,T)
Alt rs730880729(A,T;A,T)
Reference rs730880729(G;G)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23901977C>A; NC_000014.8:g.23901977C>T
CLNSRC
CLNACC RCV000158729.2, RCV000158501.1,