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rs730880853

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880853(G;T)
Make rs730880853(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431456
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880853
ebirs730880853
HLIrs730880853
Exacrs730880853
Varsomers730880853
Maprs730880853
PheGenIrs730880853
hapmaprs730880853
1000 genomesrs730880853
hgdprs730880853
ensemblrs730880853
gopubmedrs730880853
geneviewrs730880853
scholarrs730880853
googlers730880853
pharmgkbrs730880853
gwascentralrs730880853
openSNPrs730880853
23andMers730880853
23andMe allrs730880853
SNP Nexus

SNPshotrs730880853
SNPdbers730880853
MSV3drs730880853
GWAS Ctlgrs730880853
Max Magnitude0
ClinVar
Risk rs730880853(T;T)
Alt rs730880853(T;T)
Reference rs730880853(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23900665C>A
CLNSRC
CLNACC RCV000158763.1,