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rs730880787

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880787(A;A)
Make rs730880787(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23418343
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880787
ebirs730880787
HLIrs730880787
Exacrs730880787
Varsomers730880787
Maprs730880787
PheGenIrs730880787
hapmaprs730880787
1000 genomesrs730880787
hgdprs730880787
ensemblrs730880787
gopubmedrs730880787
geneviewrs730880787
scholarrs730880787
googlers730880787
pharmgkbrs730880787
gwascentralrs730880787
openSNPrs730880787
23andMers730880787
23andMe allrs730880787
SNP Nexus

SNPshotrs730880787
SNPdbers730880787
MSV3drs730880787
GWAS Ctlgrs730880787
Max Magnitude0
ClinVar
Risk rs730880787(A;A)
Alt rs730880787(A;A)
Reference rs730880787(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7 MIR208B
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23887552G>C; NC_000014.8:g.23887552G>T
CLNSRC
CLNACC RCV000213667.1, RCV000158629.3,