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rs730880866

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880866(A;A)
Make rs730880866(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429778
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880866
ebirs730880866
HLIrs730880866
Exacrs730880866
Varsomers730880866
Maprs730880866
PheGenIrs730880866
hapmaprs730880866
1000 genomesrs730880866
hgdprs730880866
ensemblrs730880866
gopubmedrs730880866
geneviewrs730880866
scholarrs730880866
googlers730880866
pharmgkbrs730880866
gwascentralrs730880866
openSNPrs730880866
23andMers730880866
23andMe allrs730880866
SNP Nexus

SNPshotrs730880866
SNPdbers730880866
MSV3drs730880866
GWAS Ctlgrs730880866
Max Magnitude0
ClinVar
Risk rs730880866(A;A)
Alt rs730880866(A;A)
Reference rs730880866(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23898987C>T
CLNSRC
CLNACC RCV000158785.1,