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

rs730880752

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880752(G;G)
Make rs730880752(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424788
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880752
ebirs730880752
HLIrs730880752
Exacrs730880752
Varsomers730880752
Maprs730880752
PheGenIrs730880752
hapmaprs730880752
1000 genomesrs730880752
hgdprs730880752
ensemblrs730880752
gopubmedrs730880752
geneviewrs730880752
scholarrs730880752
googlers730880752
pharmgkbrs730880752
gwascentralrs730880752
openSNPrs730880752
23andMers730880752
23andMe allrs730880752
SNP Nexus

SNPshotrs730880752
SNPdbers730880752
MSV3drs730880752
GWAS Ctlgrs730880752
Max Magnitude0
ClinVar
Risk rs730880752(G;G)
Alt rs730880752(G;G)
Reference rs730880752(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23893997A>C
CLNSRC
CLNACC RCV000158557.1,