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rs730880780

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880780(A;A)
Make rs730880780(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23419951
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880780
ebirs730880780
HLIrs730880780
Exacrs730880780
Varsomers730880780
Maprs730880780
PheGenIrs730880780
hapmaprs730880780
1000 genomesrs730880780
hgdprs730880780
ensemblrs730880780
gopubmedrs730880780
geneviewrs730880780
scholarrs730880780
googlers730880780
pharmgkbrs730880780
gwascentralrs730880780
openSNPrs730880780
23andMers730880780
23andMe allrs730880780
SNP Nexus

SNPshotrs730880780
SNPdbers730880780
MSV3drs730880780
GWAS Ctlgrs730880780
Max Magnitude0
ClinVar
Risk rs730880780(A;A)
Alt rs730880780(A;A)
Reference rs730880780(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23889160A>T
CLNSRC
CLNACC RCV000158615.2,