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rs730880731

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880731(C;C)
Make rs730880731(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23426063
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880731
ebirs730880731
HLIrs730880731
Exacrs730880731
Varsomers730880731
Maprs730880731
PheGenIrs730880731
hapmaprs730880731
1000 genomesrs730880731
hgdprs730880731
ensemblrs730880731
gopubmedrs730880731
geneviewrs730880731
scholarrs730880731
googlers730880731
pharmgkbrs730880731
gwascentralrs730880731
openSNPrs730880731
23andMers730880731
23andMe allrs730880731
SNP Nexus

SNPshotrs730880731
SNPdbers730880731
MSV3drs730880731
GWAS Ctlgrs730880731
Max Magnitude0
ClinVar
Risk rs730880731(C;C)
Alt rs730880731(C;C)
Reference rs730880731(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23895272A>G
CLNSRC
CLNACC RCV000158505.1,