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rs727504267

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504267(A;G)
Make rs727504267(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23432504
GeneMYH7
is asnp
is mentioned by
dbSNPrs727504267
ebirs727504267
HLIrs727504267
Exacrs727504267
Varsomers727504267
Maprs727504267
PheGenIrs727504267
hapmaprs727504267
1000 genomesrs727504267
hgdprs727504267
ensemblrs727504267
gopubmedrs727504267
geneviewrs727504267
scholarrs727504267
googlers727504267
pharmgkbrs727504267
gwascentralrs727504267
openSNPrs727504267
23andMers727504267
23andMe allrs727504267
SNP Nexus

SNPshotrs727504267
SNPdbers727504267
MSV3drs727504267
GWAS Ctlgrs727504267
Max Magnitude0
ClinVar
Risk rs727504267(G;G)
Alt rs727504267(G;G)
Reference rs727504267(A;A)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000014.8:g.23901713T>C
CLNSRC
CLNACC RCV000154253.2, RCV000223700.1,