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rs730880854

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880854(A;A)
Make rs730880854(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431438
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880854
ebirs730880854
HLIrs730880854
Exacrs730880854
Varsomers730880854
Maprs730880854
PheGenIrs730880854
hapmaprs730880854
1000 genomesrs730880854
hgdprs730880854
ensemblrs730880854
gopubmedrs730880854
geneviewrs730880854
scholarrs730880854
googlers730880854
pharmgkbrs730880854
gwascentralrs730880854
openSNPrs730880854
23andMers730880854
23andMe allrs730880854
SNP Nexus

SNPshotrs730880854
SNPdbers730880854
MSV3drs730880854
GWAS Ctlgrs730880854
Max Magnitude0
ClinVar
Risk rs730880854(A;A)
Alt rs730880854(A;A)
Reference rs730880854(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23900647G>T
CLNSRC
CLNACC RCV000158765.2,