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rs730880799

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880799(A;T)
Make rs730880799(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23417576
GeneMHRT, MIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880799
ClinGenrs730880799
ebirs730880799
HLIrs730880799
Exacrs730880799
Varsomers730880799
Maprs730880799
PheGenIrs730880799
hapmaprs730880799
1000 genomesrs730880799
hgdprs730880799
ensemblrs730880799
gopubmedrs730880799
geneviewrs730880799
scholarrs730880799
googlers730880799
pharmgkbrs730880799
gwascentralrs730880799
openSNPrs730880799
23andMers730880799
23andMe allrs730880799
SNP Nexus

SNPshotrs730880799
SNPdbers730880799
MSV3drs730880799
GWAS Ctlgrs730880799
Max Magnitude0
ClinVar
Risk rs730880799(T;T)
Alt rs730880799(T;T)
Reference Rs730880799(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B MHRT
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23886785T>A
CLNSRC
CLNACC RCV000158651.2,