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

rs730880896

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880896(A;A)
Make rs730880896(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23425327
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880896
ebirs730880896
HLIrs730880896
Exacrs730880896
Varsomers730880896
Maprs730880896
PheGenIrs730880896
hapmaprs730880896
1000 genomesrs730880896
hgdprs730880896
ensemblrs730880896
gopubmedrs730880896
geneviewrs730880896
scholarrs730880896
googlers730880896
pharmgkbrs730880896
gwascentralrs730880896
openSNPrs730880896
23andMers730880896
23andMe allrs730880896
SNP Nexus

SNPshotrs730880896
SNPdbers730880896
MSV3drs730880896
GWAS Ctlgrs730880896
Max Magnitude0
ClinVar
Risk rs730880896(A;A)
Alt rs730880896(A;A)
Reference rs730880896(G;G)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MYH7
CLNDBN not provided not specified
Reversed 1
HGVS NC_000014.8:g.23894536C>T
CLNSRC
CLNACC RCV000158841.1, RCV000168871.1,