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rs730880805

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880805(A;G)
Make rs730880805(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23416293
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880805
ebirs730880805
HLIrs730880805
Exacrs730880805
Varsomers730880805
Maprs730880805
PheGenIrs730880805
hapmaprs730880805
1000 genomesrs730880805
hgdprs730880805
ensemblrs730880805
gopubmedrs730880805
geneviewrs730880805
scholarrs730880805
googlers730880805
pharmgkbrs730880805
gwascentralrs730880805
openSNPrs730880805
23andMers730880805
23andMe allrs730880805
SNP Nexus

SNPshotrs730880805
SNPdbers730880805
MSV3drs730880805
GWAS Ctlgrs730880805
Max Magnitude0
ClinVar
Risk rs730880805(G;G)
Alt rs730880805(G;G)
Reference rs730880805(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7 MHRT
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23885502T>C
CLNSRC
CLNACC RCV000158665.1,