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rs730880927

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880927(G;G)
Make rs730880927(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429046
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880927
ebirs730880927
HLIrs730880927
Exacrs730880927
Varsomers730880927
Maprs730880927
PheGenIrs730880927
hapmaprs730880927
1000 genomesrs730880927
hgdprs730880927
ensemblrs730880927
gopubmedrs730880927
geneviewrs730880927
scholarrs730880927
googlers730880927
pharmgkbrs730880927
gwascentralrs730880927
openSNPrs730880927
23andMers730880927
23andMe allrs730880927
SNP Nexus

SNPshotrs730880927
SNPdbers730880927
MSV3drs730880927
GWAS Ctlgrs730880927
Max Magnitude0
ClinVar
Risk rs730880927(G;G)
Alt rs730880927(G;G)
Reference rs730880927(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23898255A>C
CLNSRC
CLNACC RCV000158887.1,