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

rs730880798

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880798(A;A)
Make rs730880798(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23417586
GeneMHRT, MIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880798
ebirs730880798
HLIrs730880798
Exacrs730880798
Varsomers730880798
Maprs730880798
PheGenIrs730880798
hapmaprs730880798
1000 genomesrs730880798
hgdprs730880798
ensemblrs730880798
gopubmedrs730880798
geneviewrs730880798
scholarrs730880798
googlers730880798
pharmgkbrs730880798
gwascentralrs730880798
openSNPrs730880798
23andMers730880798
23andMe allrs730880798
SNP Nexus

SNPshotrs730880798
SNPdbers730880798
MSV3drs730880798
GWAS Ctlgrs730880798
Max Magnitude0
ClinVar
Risk rs730880798(A;A)
Alt rs730880798(A;A)
Reference rs730880798(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MHRT MIR208B
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23886795C>T
CLNSRC
CLNACC RCV000158649.2,