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rs730880766

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880766(G;T)
Make rs730880766(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23422299
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880766
ebirs730880766
HLIrs730880766
Exacrs730880766
Varsomers730880766
Maprs730880766
PheGenIrs730880766
hapmaprs730880766
1000 genomesrs730880766
hgdprs730880766
ensemblrs730880766
gopubmedrs730880766
geneviewrs730880766
scholarrs730880766
googlers730880766
pharmgkbrs730880766
gwascentralrs730880766
openSNPrs730880766
23andMers730880766
23andMe allrs730880766
SNP Nexus

SNPshotrs730880766
SNPdbers730880766
MSV3drs730880766
GWAS Ctlgrs730880766
Max Magnitude0
ClinVar
Risk rs730880766(T;T)
Alt rs730880766(T;T)
Reference rs730880766(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23891508C>A
CLNSRC
CLNACC RCV000158586.1,