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rs730880910

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880910(C;T)
Make rs730880910(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23418235
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880910
ebirs730880910
HLIrs730880910
Exacrs730880910
Varsomers730880910
Maprs730880910
PheGenIrs730880910
hapmaprs730880910
1000 genomesrs730880910
hgdprs730880910
ensemblrs730880910
gopubmedrs730880910
geneviewrs730880910
scholarrs730880910
googlers730880910
pharmgkbrs730880910
gwascentralrs730880910
openSNPrs730880910
23andMers730880910
23andMe allrs730880910
SNP Nexus

SNPshotrs730880910
SNPdbers730880910
MSV3drs730880910
GWAS Ctlgrs730880910
Max Magnitude0
ClinVar
Risk rs730880910(T;T)
Alt rs730880910(T;T)
Reference rs730880910(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23887444G>A
CLNSRC
CLNACC RCV000158864.1,