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rs730880753

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880753(A;A)
Make rs730880753(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424133
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880753
ebirs730880753
HLIrs730880753
Exacrs730880753
Varsomers730880753
Maprs730880753
PheGenIrs730880753
hapmaprs730880753
1000 genomesrs730880753
hgdprs730880753
ensemblrs730880753
gopubmedrs730880753
geneviewrs730880753
scholarrs730880753
googlers730880753
pharmgkbrs730880753
gwascentralrs730880753
openSNPrs730880753
23andMers730880753
23andMe allrs730880753
SNP Nexus

SNPshotrs730880753
SNPdbers730880753
MSV3drs730880753
GWAS Ctlgrs730880753
Max Magnitude0
ClinVar
Risk rs730880753(A;A)
Alt rs730880753(A;A)
Reference rs730880753(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23893342G>T
CLNSRC
CLNACC RCV000158561.2,