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rs730880921

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880921(C;G)
Make rs730880921(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431592
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880921
ebirs730880921
HLIrs730880921
Exacrs730880921
Varsomers730880921
Maprs730880921
PheGenIrs730880921
hapmaprs730880921
1000 genomesrs730880921
hgdprs730880921
ensemblrs730880921
gopubmedrs730880921
geneviewrs730880921
scholarrs730880921
googlers730880921
pharmgkbrs730880921
gwascentralrs730880921
openSNPrs730880921
23andMers730880921
23andMe allrs730880921
SNP Nexus

SNPshotrs730880921
SNPdbers730880921
MSV3drs730880921
GWAS Ctlgrs730880921
Max Magnitude0
ClinVar
Risk rs730880921(G;G)
Alt rs730880921(G;G)
Reference rs730880921(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23900801G>C
CLNSRC
CLNACC RCV000158880.1,