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rs1057524857

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524857(A;A)
Make rs1057524857(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position23425977
GeneMYH7
is asnp
is mentioned by
dbSNPrs1057524857
dbSNP (old)rs1057524857
ClinGenrs1057524857
ebirs1057524857
HLIrs1057524857
Exacrs1057524857
Gnomadrs1057524857
Varsomers1057524857
Maprs1057524857
PheGenIrs1057524857
Biobankrs1057524857
1000 genomesrs1057524857
hgdprs1057524857
ensemblrs1057524857
gopubmedrs1057524857
geneviewrs1057524857
scholarrs1057524857
googlers1057524857
pharmgkbrs1057524857
gwascentralrs1057524857
openSNPrs1057524857
23andMers1057524857
23andMe allrs1057524857
SNPshotrs1057524857
SNPdbers1057524857
MSV3drs1057524857
GWAS Ctlgrs1057524857
Max Magnitude0
ClinVar
Risk rs1057524857(A;A)
Alt rs1057524857(A;A)
Reference Rs1057524857(G;G)
Significance Probable-Pathogenic
Disease not provided Hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN not provided Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23895186C>T
CLNSRC
CLNACC RCV000429496.1, RCV000460699.1,