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rs730880891

From SNPedia

Orientationminus
Geno Mag Summary
(TGC;TGC) 0 common in clinvar
Make rs730880891(-;-)
Make rs730880891(-;TGC)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23417664
GeneMHRT, MIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880891
ebirs730880891
HLIrs730880891
Exacrs730880891
Varsomers730880891
Maprs730880891
PheGenIrs730880891
hapmaprs730880891
1000 genomesrs730880891
hgdprs730880891
ensemblrs730880891
gopubmedrs730880891
geneviewrs730880891
scholarrs730880891
googlers730880891
pharmgkbrs730880891
gwascentralrs730880891
openSNPrs730880891
23andMers730880891
23andMe allrs730880891
SNP Nexus

SNPshotrs730880891
SNPdbers730880891
MSV3drs730880891
GWAS Ctlgrs730880891
Max Magnitude0
ClinVar
Risk rs730880891(;)
Alt rs730880891(;)
Reference rs730880891(TGC;TGC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B MHRT
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23886873_23886875delGCA
CLNSRC
CLNACC RCV000158833.1,