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rs730880791

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880791(A;A)
Make rs730880791(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23418253
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880791
ebirs730880791
HLIrs730880791
Exacrs730880791
Varsomers730880791
Maprs730880791
PheGenIrs730880791
hapmaprs730880791
1000 genomesrs730880791
hgdprs730880791
ensemblrs730880791
gopubmedrs730880791
geneviewrs730880791
scholarrs730880791
googlers730880791
pharmgkbrs730880791
gwascentralrs730880791
openSNPrs730880791
23andMers730880791
23andMe allrs730880791
SNP Nexus

SNPshotrs730880791
SNPdbers730880791
MSV3drs730880791
GWAS Ctlgrs730880791
Max Magnitude0
ClinVar
Risk rs730880791(A;A)
Alt rs730880791(A;A)
Reference rs730880791(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23887462C>T
CLNSRC
CLNACC RCV000158635.2,