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

rs730880788

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880788(C;C)
Make rs730880788(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23418309
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880788
ebirs730880788
HLIrs730880788
Exacrs730880788
Varsomers730880788
Maprs730880788
PheGenIrs730880788
hapmaprs730880788
1000 genomesrs730880788
hgdprs730880788
ensemblrs730880788
gopubmedrs730880788
geneviewrs730880788
scholarrs730880788
googlers730880788
pharmgkbrs730880788
gwascentralrs730880788
openSNPrs730880788
23andMers730880788
23andMe allrs730880788
SNP Nexus

SNPshotrs730880788
SNPdbers730880788
MSV3drs730880788
GWAS Ctlgrs730880788
Max Magnitude0
ClinVar
Risk rs730880788(C;C)
Alt rs730880788(C;C)
Reference rs730880788(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23887518A>G
CLNSRC
CLNACC RCV000158631.1,