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rs730880934

From SNPedia

Orientationminus
Geno Mag Summary
(CTG;CTG) 0 common in clinvar
Make rs730880934(-;-)
Make rs730880934(-;CTG)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23419246
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880934
ebirs730880934
HLIrs730880934
Exacrs730880934
Varsomers730880934
Maprs730880934
PheGenIrs730880934
hapmaprs730880934
1000 genomesrs730880934
hgdprs730880934
ensemblrs730880934
gopubmedrs730880934
geneviewrs730880934
scholarrs730880934
googlers730880934
pharmgkbrs730880934
gwascentralrs730880934
openSNPrs730880934
23andMers730880934
23andMe allrs730880934
SNP Nexus

SNPshotrs730880934
SNPdbers730880934
MSV3drs730880934
GWAS Ctlgrs730880934
Max Magnitude0
ClinVar
Risk rs730880934(;)
Alt rs730880934(;)
Reference rs730880934(CTG;CTG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23888455_23888457delCAG
CLNSRC
CLNACC RCV000158895.1,