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rs730880742

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880742(A;T)
Make rs730880742(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424984
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880742
ebirs730880742
HLIrs730880742
Exacrs730880742
Varsomers730880742
Maprs730880742
PheGenIrs730880742
hapmaprs730880742
1000 genomesrs730880742
hgdprs730880742
ensemblrs730880742
gopubmedrs730880742
geneviewrs730880742
scholarrs730880742
googlers730880742
pharmgkbrs730880742
gwascentralrs730880742
openSNPrs730880742
23andMers730880742
23andMe allrs730880742
SNP Nexus

SNPshotrs730880742
SNPdbers730880742
MSV3drs730880742
GWAS Ctlgrs730880742
Max Magnitude0
ClinVar
Risk rs730880742(C,T;C,T)
Alt rs730880742(C,T;C,T)
Reference rs730880742(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23894193T>A; NC_000014.8:g.23894193T>G
CLNSRC
CLNACC RCV000158539.2, RCV000158840.1,