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rs730880884

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880884(G;G)
Make rs730880884(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23426803
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880884
ebirs730880884
HLIrs730880884
Exacrs730880884
Varsomers730880884
Maprs730880884
PheGenIrs730880884
hapmaprs730880884
1000 genomesrs730880884
hgdprs730880884
ensemblrs730880884
gopubmedrs730880884
geneviewrs730880884
scholarrs730880884
googlers730880884
pharmgkbrs730880884
gwascentralrs730880884
openSNPrs730880884
23andMers730880884
23andMe allrs730880884
SNP Nexus

SNPshotrs730880884
SNPdbers730880884
MSV3drs730880884
GWAS Ctlgrs730880884
Max Magnitude0
ClinVar
Risk rs730880884(G;G)
Alt rs730880884(G;G)
Reference rs730880884(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23896012A>C
CLNSRC
CLNACC RCV000158825.1,