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rs730880790

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880790(C;C)
Make rs730880790(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23418256
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880790
ebirs730880790
HLIrs730880790
Exacrs730880790
Varsomers730880790
Maprs730880790
PheGenIrs730880790
hapmaprs730880790
1000 genomesrs730880790
hgdprs730880790
ensemblrs730880790
gopubmedrs730880790
geneviewrs730880790
scholarrs730880790
googlers730880790
pharmgkbrs730880790
gwascentralrs730880790
openSNPrs730880790
23andMers730880790
23andMe allrs730880790
SNP Nexus

SNPshotrs730880790
SNPdbers730880790
MSV3drs730880790
GWAS Ctlgrs730880790
Max Magnitude0
ClinVar
Risk rs730880790(C;C)
Alt rs730880790(C;C)
Reference rs730880790(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23887465A>G
CLNSRC
CLNACC RCV000158634.1,