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rs730880792

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880792(A;A)
Make rs730880792(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23418220
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880792
ebirs730880792
HLIrs730880792
Exacrs730880792
Varsomers730880792
Maprs730880792
PheGenIrs730880792
hapmaprs730880792
1000 genomesrs730880792
hgdprs730880792
ensemblrs730880792
gopubmedrs730880792
geneviewrs730880792
scholarrs730880792
googlers730880792
pharmgkbrs730880792
gwascentralrs730880792
openSNPrs730880792
23andMers730880792
23andMe allrs730880792
SNP Nexus

SNPshotrs730880792
SNPdbers730880792
MSV3drs730880792
GWAS Ctlgrs730880792
Max Magnitude0
ClinVar
Risk rs730880792(A,C;A,C)
Alt rs730880792(A,C;A,C)
Reference rs730880792(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7 MIR208B
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23887429C>T
CLNSRC
CLNACC RCV000158638.2,