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rs730880749

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880749(A;G)
Make rs730880749(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424855
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880749
ebirs730880749
HLIrs730880749
Exacrs730880749
Varsomers730880749
Maprs730880749
PheGenIrs730880749
hapmaprs730880749
1000 genomesrs730880749
hgdprs730880749
ensemblrs730880749
gopubmedrs730880749
geneviewrs730880749
scholarrs730880749
googlers730880749
pharmgkbrs730880749
gwascentralrs730880749
openSNPrs730880749
23andMers730880749
23andMe allrs730880749
SNP Nexus

SNPshotrs730880749
SNPdbers730880749
MSV3drs730880749
GWAS Ctlgrs730880749
Max Magnitude0
ClinVar
Risk rs730880749(G;G)
Alt rs730880749(G;G)
Reference rs730880749(A;A)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MYH7
CLNDBN not provided not specified
Reversed 1
HGVS NC_000014.8:g.23894064T>C
CLNSRC
CLNACC RCV000158550.2, RCV000223827.1,