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rs730880889

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730880889(-;-)
Make rs730880889(-;GGGAAG)
Make rs730880889(GGGAAG;GGGAAG)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23419907
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880889
ebirs730880889
HLIrs730880889
Exacrs730880889
Varsomers730880889
Maprs730880889
PheGenIrs730880889
hapmaprs730880889
1000 genomesrs730880889
hgdprs730880889
ensemblrs730880889
gopubmedrs730880889
geneviewrs730880889
scholarrs730880889
googlers730880889
pharmgkbrs730880889
gwascentralrs730880889
openSNPrs730880889
23andMers730880889
23andMe allrs730880889
SNP Nexus

SNPshotrs730880889
SNPdbers730880889
MSV3drs730880889
GWAS Ctlgrs730880889
Max Magnitude0
ClinVar
Risk rs730880889(GGGAAG;GGGAAG)
Alt rs730880889(GGGAAG;GGGAAG)
Reference rs730880889(;)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7 MIR208B
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23889116_23889117insCTTCCC
CLNSRC
CLNACC RCV000158831.1,