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rs730880907

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880907(A;G)
Make rs730880907(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23418286
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880907
ebirs730880907
HLIrs730880907
Exacrs730880907
Varsomers730880907
Maprs730880907
PheGenIrs730880907
hapmaprs730880907
1000 genomesrs730880907
hgdprs730880907
ensemblrs730880907
gopubmedrs730880907
geneviewrs730880907
scholarrs730880907
googlers730880907
pharmgkbrs730880907
gwascentralrs730880907
openSNPrs730880907
23andMers730880907
23andMe allrs730880907
SNP Nexus

SNPshotrs730880907
SNPdbers730880907
MSV3drs730880907
GWAS Ctlgrs730880907
Max Magnitude0
ClinVar
Risk rs730880907(G;G)
Alt rs730880907(G;G)
Reference rs730880907(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23887495T>C
CLNSRC
CLNACC RCV000158861.1,