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rs727504274

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504274(A;A)
Make rs727504274(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23420225
GeneMYH7
is asnp
is mentioned by
dbSNPrs727504274
ebirs727504274
HLIrs727504274
Exacrs727504274
Varsomers727504274
Maprs727504274
PheGenIrs727504274
hapmaprs727504274
1000 genomesrs727504274
hgdprs727504274
ensemblrs727504274
gopubmedrs727504274
geneviewrs727504274
scholarrs727504274
googlers727504274
pharmgkbrs727504274
gwascentralrs727504274
openSNPrs727504274
23andMers727504274
23andMe allrs727504274
SNP Nexus

SNPshotrs727504274
SNPdbers727504274
MSV3drs727504274
GWAS Ctlgrs727504274
Max Magnitude0
ClinVar
Risk rs727504274(A;A)
Alt rs727504274(A;A)
Reference rs727504274(G;G)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not provided Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy not provided Familial hypertrophic cardiomyopathy 1
Reversed 1
HGVS NC_000014.8:g.23889434C>T
CLNSRC
CLNACC RCV000154273.2, RCV000158602.2, RCV000168887.1,