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rs730880750

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880750(C;T)
Make rs730880750(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424843
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880750
ebirs730880750
HLIrs730880750
Exacrs730880750
Varsomers730880750
Maprs730880750
PheGenIrs730880750
hapmaprs730880750
1000 genomesrs730880750
hgdprs730880750
ensemblrs730880750
gopubmedrs730880750
geneviewrs730880750
scholarrs730880750
googlers730880750
pharmgkbrs730880750
gwascentralrs730880750
openSNPrs730880750
23andMers730880750
23andMe allrs730880750
SNP Nexus

SNPshotrs730880750
SNPdbers730880750
MSV3drs730880750
GWAS Ctlgrs730880750
Max Magnitude0
ClinVar
Risk rs730880750(A,T;A,T)
Alt rs730880750(A,T;A,T)
Reference rs730880750(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23894052G>T
CLNSRC
CLNACC RCV000168874.1,