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rs730880796

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880796(C;T)
Make rs730880796(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23417618
GeneMHRT, MIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880796
ebirs730880796
HLIrs730880796
Exacrs730880796
Varsomers730880796
Maprs730880796
PheGenIrs730880796
hapmaprs730880796
1000 genomesrs730880796
hgdprs730880796
ensemblrs730880796
gopubmedrs730880796
geneviewrs730880796
scholarrs730880796
googlers730880796
pharmgkbrs730880796
gwascentralrs730880796
openSNPrs730880796
23andMers730880796
23andMe allrs730880796
SNP Nexus

SNPshotrs730880796
SNPdbers730880796
MSV3drs730880796
GWAS Ctlgrs730880796
Max Magnitude0
ClinVar
Risk rs730880796(T;T)
Alt rs730880796(T;T)
Reference rs730880796(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B MHRT
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23886827G>A
CLNSRC
CLNACC RCV000158645.2,