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rs1057517773

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517773(A;A)
Make rs1057517773(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position23431641
GeneMYH7
is asnp
is mentioned by
dbSNPrs1057517773
dbSNP (old)rs1057517773
ClinGenrs1057517773
ebirs1057517773
HLIrs1057517773
Exacrs1057517773
Gnomadrs1057517773
Varsomers1057517773
LitVarrs1057517773
Maprs1057517773
PheGenIrs1057517773
Biobankrs1057517773
1000 genomesrs1057517773
hgdprs1057517773
ensemblrs1057517773
gopubmedrs1057517773
geneviewrs1057517773
scholarrs1057517773
googlers1057517773
pharmgkbrs1057517773
gwascentralrs1057517773
openSNPrs1057517773
23andMers1057517773
23andMe allrs1057517773
SNPshotrs1057517773
SNPdbers1057517773
MSV3drs1057517773
GWAS Ctlgrs1057517773
Max Magnitude0
ClinVar
Risk rs1057517773(A;A)
Alt rs1057517773(A;A)
Reference Rs1057517773(G;G)
Significance Probable-Pathogenic
Disease not specified Hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN not specified Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23900850C>T
CLNSRC
CLNACC RCV000412779.1, RCV000457952.1,