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rs730880762

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880762(C;G)
Make rs730880762(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23423636
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880762
ebirs730880762
HLIrs730880762
Exacrs730880762
Varsomers730880762
Maprs730880762
PheGenIrs730880762
hapmaprs730880762
1000 genomesrs730880762
hgdprs730880762
ensemblrs730880762
gopubmedrs730880762
geneviewrs730880762
scholarrs730880762
googlers730880762
pharmgkbrs730880762
gwascentralrs730880762
openSNPrs730880762
23andMers730880762
23andMe allrs730880762
SNP Nexus

SNPshotrs730880762
SNPdbers730880762
MSV3drs730880762
GWAS Ctlgrs730880762
Max Magnitude0
ClinVar
Risk rs730880762(G;G)
Alt rs730880762(G;G)
Reference rs730880762(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23892845G>C
CLNSRC
CLNACC RCV000158582.1,