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rs730880733

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880733(C;C)
Make rs730880733(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23425966
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880733
ebirs730880733
HLIrs730880733
Exacrs730880733
Varsomers730880733
Maprs730880733
PheGenIrs730880733
hapmaprs730880733
1000 genomesrs730880733
hgdprs730880733
ensemblrs730880733
gopubmedrs730880733
geneviewrs730880733
scholarrs730880733
googlers730880733
pharmgkbrs730880733
gwascentralrs730880733
openSNPrs730880733
23andMers730880733
23andMe allrs730880733
SNP Nexus

SNPshotrs730880733
SNPdbers730880733
MSV3drs730880733
GWAS Ctlgrs730880733
Max Magnitude0
ClinVar
Risk rs730880733(C;C)
Alt rs730880733(C;C)
Reference rs730880733(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23895175C>G
CLNSRC
CLNACC RCV000158514.2,