Have questions? Visit https://www.reddit.com/r/SNPedia

rs730880826

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880826(C;C)
Make rs730880826(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23433704
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880826
ebirs730880826
HLIrs730880826
Exacrs730880826
Varsomers730880826
Maprs730880826
PheGenIrs730880826
hapmaprs730880826
1000 genomesrs730880826
hgdprs730880826
ensemblrs730880826
gopubmedrs730880826
geneviewrs730880826
scholarrs730880826
googlers730880826
pharmgkbrs730880826
gwascentralrs730880826
openSNPrs730880826
23andMers730880826
23andMe allrs730880826
SNP Nexus

SNPshotrs730880826
SNPdbers730880826
MSV3drs730880826
GWAS Ctlgrs730880826
Max Magnitude0
ClinVar
Risk rs730880826(C;C)
Alt rs730880826(C;C)
Reference rs730880826(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23902913C>G
CLNSRC
CLNACC RCV000158720.1,