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rs730880929

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880929(C;C)
Make rs730880929(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23428507
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880929
ebirs730880929
HLIrs730880929
Exacrs730880929
Varsomers730880929
Maprs730880929
PheGenIrs730880929
hapmaprs730880929
1000 genomesrs730880929
hgdprs730880929
ensemblrs730880929
gopubmedrs730880929
geneviewrs730880929
scholarrs730880929
googlers730880929
pharmgkbrs730880929
gwascentralrs730880929
openSNPrs730880929
23andMers730880929
23andMe allrs730880929
SNP Nexus

SNPshotrs730880929
SNPdbers730880929
MSV3drs730880929
GWAS Ctlgrs730880929
Max Magnitude0
ClinVar
Risk rs730880929(C;C)
Alt rs730880929(C;C)
Reference rs730880929(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23897716A>G
CLNSRC
CLNACC RCV000158889.1,