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rs730880743

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880743(A;C)
Make rs730880743(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424975
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880743
ebirs730880743
HLIrs730880743
Exacrs730880743
Varsomers730880743
Maprs730880743
PheGenIrs730880743
hapmaprs730880743
1000 genomesrs730880743
hgdprs730880743
ensemblrs730880743
gopubmedrs730880743
geneviewrs730880743
scholarrs730880743
googlers730880743
pharmgkbrs730880743
gwascentralrs730880743
openSNPrs730880743
23andMers730880743
23andMe allrs730880743
SNP Nexus

SNPshotrs730880743
SNPdbers730880743
MSV3drs730880743
GWAS Ctlgrs730880743
Max Magnitude0
ClinVar
Risk rs730880743(C;C)
Alt rs730880743(C;C)
Reference rs730880743(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23894184T>G
CLNSRC
CLNACC RCV000158540.2,