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rs730880859

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880859(A;A)
Make rs730880859(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23430595
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880859
ClinGenrs730880859
ebirs730880859
HLIrs730880859
Exacrs730880859
Varsomers730880859
Maprs730880859
PheGenIrs730880859
hapmaprs730880859
1000 genomesrs730880859
hgdprs730880859
ensemblrs730880859
gopubmedrs730880859
geneviewrs730880859
scholarrs730880859
googlers730880859
pharmgkbrs730880859
gwascentralrs730880859
openSNPrs730880859
23andMers730880859
23andMe allrs730880859
SNP Nexus

SNPshotrs730880859
SNPdbers730880859
MSV3drs730880859
GWAS Ctlgrs730880859
Max Magnitude0
ClinVar
Risk rs730880859(A;A)
Alt rs730880859(A;A)
Reference Rs730880859(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23899804A>T
CLNSRC
CLNACC RCV000158773.1,