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rs730880764

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880764(A;A)
Make rs730880764(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23423609
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880764
ebirs730880764
HLIrs730880764
Exacrs730880764
Varsomers730880764
Maprs730880764
PheGenIrs730880764
hapmaprs730880764
1000 genomesrs730880764
hgdprs730880764
ensemblrs730880764
gopubmedrs730880764
geneviewrs730880764
scholarrs730880764
googlers730880764
pharmgkbrs730880764
gwascentralrs730880764
openSNPrs730880764
23andMers730880764
23andMe allrs730880764
SNP Nexus

SNPshotrs730880764
SNPdbers730880764
MSV3drs730880764
GWAS Ctlgrs730880764
Max Magnitude0
ClinVar
Risk rs730880764(A;A)
Alt rs730880764(A;A)
Reference rs730880764(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23892818C>T
CLNSRC
CLNACC RCV000158584.1,