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rs730880778

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880778(A;A)
Make rs730880778(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23419979
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880778
ebirs730880778
HLIrs730880778
Exacrs730880778
Varsomers730880778
Maprs730880778
PheGenIrs730880778
hapmaprs730880778
1000 genomesrs730880778
hgdprs730880778
ensemblrs730880778
gopubmedrs730880778
geneviewrs730880778
scholarrs730880778
googlers730880778
pharmgkbrs730880778
gwascentralrs730880778
openSNPrs730880778
23andMers730880778
23andMe allrs730880778
SNP Nexus

SNPshotrs730880778
SNPdbers730880778
MSV3drs730880778
GWAS Ctlgrs730880778
Max Magnitude0
ClinVar
Risk rs730880778(A;A)
Alt rs730880778(A;A)
Reference rs730880778(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7 MIR208B
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23889188C>T
CLNSRC
CLNACC RCV000168890.2,