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rs2754158

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2754158(C;C)
Make rs2754158(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424876
GeneMYH7
is asnp
is mentioned by
dbSNPrs2754158
ebirs2754158
HLIrs2754158
Exacrs2754158
Varsomers2754158
Maprs2754158
PheGenIrs2754158
hapmaprs2754158
1000 genomesrs2754158
hgdprs2754158
ensemblrs2754158
gopubmedrs2754158
geneviewrs2754158
scholarrs2754158
googlers2754158
pharmgkbrs2754158
gwascentralrs2754158
openSNPrs2754158
23andMers2754158
23andMe allrs2754158
SNP Nexus

SNPshotrs2754158
SNPdbers2754158
MSV3drs2754158
GWAS Ctlgrs2754158
Max Magnitude0
ClinVar
Risk rs2754158(A,C,T;A,C,T)
Alt rs2754158(A,C,T;A,C,T)
Reference rs2754158(G;G)
Significance Probable-Pathogenic
Disease not specified Familial hypertrophic cardiomyopathy 1 not provided
Variation info
Gene MYH7
CLNDBN not specified Familial hypertrophic cardiomyopathy 1 not provided
Reversed 0
HGVS NC_000014.8:g.23894085G>A; NC_000014.8:g.23894085G>C; NC_000014.8:g.23894085G>T
CLNSRC
CLNACC RCV000151262.2, RCV000201448.1, RCV000225738.1, RCV000151263.1, RCV000151264.2,