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rs730880736

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880736(A;A)
Make rs730880736(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23425359
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880736
ebirs730880736
HLIrs730880736
Exacrs730880736
Varsomers730880736
Maprs730880736
PheGenIrs730880736
hapmaprs730880736
1000 genomesrs730880736
hgdprs730880736
ensemblrs730880736
gopubmedrs730880736
geneviewrs730880736
scholarrs730880736
googlers730880736
pharmgkbrs730880736
gwascentralrs730880736
openSNPrs730880736
23andMers730880736
23andMe allrs730880736
SNP Nexus

SNPshotrs730880736
SNPdbers730880736
MSV3drs730880736
GWAS Ctlgrs730880736
Max Magnitude0
ClinVar
Risk rs730880736(A;A)
Alt rs730880736(A;A)
Reference rs730880736(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23894568G>T
CLNSRC
CLNACC RCV000158528.1,