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rs1060501432

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060501432(G;G)
Make rs1060501432(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position23425973
GeneMYH7
is asnp
is mentioned by
dbSNPrs1060501432
dbSNP (old)rs1060501432
ClinGenrs1060501432
ebirs1060501432
HLIrs1060501432
Exacrs1060501432
Gnomadrs1060501432
Varsomers1060501432
Maprs1060501432
PheGenIrs1060501432
Biobankrs1060501432
1000 genomesrs1060501432
hgdprs1060501432
ensemblrs1060501432
gopubmedrs1060501432
geneviewrs1060501432
scholarrs1060501432
googlers1060501432
pharmgkbrs1060501432
gwascentralrs1060501432
openSNPrs1060501432
23andMers1060501432
23andMe allrs1060501432
SNPshotrs1060501432
SNPdbers1060501432
MSV3drs1060501432
GWAS Ctlgrs1060501432
Max Magnitude0
ClinVar
Risk rs1060501432(G;G)
Alt rs1060501432(G;G)
Reference Rs1060501432(T;T)
Significance Probable-Pathogenic
Disease Hypertrophic cardiomyopathy not provided
Variation info
Gene MYH7
CLNDBN Hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000014.8:g.23895182A>C
CLNSRC
CLNACC RCV000473139.1, RCV000486340.1,