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rs1060505018

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060505018(G;T)
Make rs1060505018(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position23424817
GeneMYH7
is asnp
is mentioned by
dbSNPrs1060505018
dbSNP (old)rs1060505018
ClinGenrs1060505018
ebirs1060505018
HLIrs1060505018
Exacrs1060505018
Gnomadrs1060505018
Varsomers1060505018
Maprs1060505018
PheGenIrs1060505018
Biobankrs1060505018
1000 genomesrs1060505018
hgdprs1060505018
ensemblrs1060505018
gopubmedrs1060505018
geneviewrs1060505018
scholarrs1060505018
googlers1060505018
pharmgkbrs1060505018
gwascentralrs1060505018
openSNPrs1060505018
23andMers1060505018
23andMe allrs1060505018
SNPshotrs1060505018
SNPdbers1060505018
MSV3drs1060505018
GWAS Ctlgrs1060505018
Max Magnitude0
ClinVar
Risk rs1060505018(T;T)
Alt rs1060505018(T;T)
Reference Rs1060505018(G;G)
Significance Pathogenic
Disease Hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23894026C>A
CLNSRC
CLNACC RCV000477668.1,