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rs730880833

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880833(C;C)
Make rs730880833(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23433088
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880833
ebirs730880833
HLIrs730880833
Exacrs730880833
Varsomers730880833
Maprs730880833
PheGenIrs730880833
hapmaprs730880833
1000 genomesrs730880833
hgdprs730880833
ensemblrs730880833
gopubmedrs730880833
geneviewrs730880833
scholarrs730880833
googlers730880833
pharmgkbrs730880833
gwascentralrs730880833
openSNPrs730880833
23andMers730880833
23andMe allrs730880833
SNP Nexus

SNPshotrs730880833
SNPdbers730880833
MSV3drs730880833
GWAS Ctlgrs730880833
Max Magnitude0
ClinVar
Risk rs730880833(C;C)
Alt rs730880833(C;C)
Reference rs730880833(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23902297A>G
CLNSRC
CLNACC RCV000158728.1,