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rs730880774

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880774(A;A)
Make rs730880774(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23420147
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880774
ebirs730880774
HLIrs730880774
Exacrs730880774
Varsomers730880774
Maprs730880774
PheGenIrs730880774
hapmaprs730880774
1000 genomesrs730880774
hgdprs730880774
ensemblrs730880774
gopubmedrs730880774
geneviewrs730880774
scholarrs730880774
googlers730880774
pharmgkbrs730880774
gwascentralrs730880774
openSNPrs730880774
23andMers730880774
23andMe allrs730880774
SNP Nexus

SNPshotrs730880774
SNPdbers730880774
MSV3drs730880774
GWAS Ctlgrs730880774
Max Magnitude0
ClinVar
Risk rs730880774(A;A)
Alt rs730880774(A;A)
Reference rs730880774(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23889356C>T
CLNSRC
CLNACC RCV000158606.2,