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rs730880745

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880745(C;C)
Make rs730880745(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424953
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880745
ebirs730880745
HLIrs730880745
Exacrs730880745
Varsomers730880745
Maprs730880745
PheGenIrs730880745
hapmaprs730880745
1000 genomesrs730880745
hgdprs730880745
ensemblrs730880745
gopubmedrs730880745
geneviewrs730880745
scholarrs730880745
googlers730880745
pharmgkbrs730880745
gwascentralrs730880745
openSNPrs730880745
23andMers730880745
23andMe allrs730880745
SNP Nexus

SNPshotrs730880745
SNPdbers730880745
MSV3drs730880745
GWAS Ctlgrs730880745
Max Magnitude0
ClinVar
Risk rs730880745(C;C)
Alt rs730880745(C;C)
Reference rs730880745(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23894162A>G
CLNSRC
CLNACC RCV000158542.2,