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rs730880758

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880758(A;C)
Make rs730880758(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424095
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880758
ebirs730880758
HLIrs730880758
Exacrs730880758
Varsomers730880758
Maprs730880758
PheGenIrs730880758
hapmaprs730880758
1000 genomesrs730880758
hgdprs730880758
ensemblrs730880758
gopubmedrs730880758
geneviewrs730880758
scholarrs730880758
googlers730880758
pharmgkbrs730880758
gwascentralrs730880758
openSNPrs730880758
23andMers730880758
23andMe allrs730880758
SNP Nexus

SNPshotrs730880758
SNPdbers730880758
MSV3drs730880758
GWAS Ctlgrs730880758
Max Magnitude0
ClinVar
Risk rs730880758(C;C)
Alt rs730880758(C;C)
Reference rs730880758(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23893304T>G
CLNSRC
CLNACC RCV000158571.2,