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rs730880782

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880782(C;G)
Make rs730880782(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23419944
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880782
ebirs730880782
HLIrs730880782
Exacrs730880782
Varsomers730880782
Maprs730880782
PheGenIrs730880782
hapmaprs730880782
1000 genomesrs730880782
hgdprs730880782
ensemblrs730880782
gopubmedrs730880782
geneviewrs730880782
scholarrs730880782
googlers730880782
pharmgkbrs730880782
gwascentralrs730880782
openSNPrs730880782
23andMers730880782
23andMe allrs730880782
SNP Nexus

SNPshotrs730880782
SNPdbers730880782
MSV3drs730880782
GWAS Ctlgrs730880782
Max Magnitude0
ClinVar
Risk rs730880782(G;G)
Alt rs730880782(G;G)
Reference rs730880782(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23889153G>C
CLNSRC
CLNACC RCV000158617.1,