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rs727504238

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504238(A;G)
Make rs727504238(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23427746
GeneMYH7
is asnp
is mentioned by
dbSNPrs727504238
ebirs727504238
HLIrs727504238
Exacrs727504238
Varsomers727504238
Maprs727504238
PheGenIrs727504238
hapmaprs727504238
1000 genomesrs727504238
hgdprs727504238
ensemblrs727504238
gopubmedrs727504238
geneviewrs727504238
scholarrs727504238
googlers727504238
pharmgkbrs727504238
gwascentralrs727504238
openSNPrs727504238
23andMers727504238
23andMe allrs727504238
SNP Nexus

SNPshotrs727504238
SNPdbers727504238
MSV3drs727504238
GWAS Ctlgrs727504238
Max Magnitude0
ClinVar
Risk rs727504238(G;G)
Alt rs727504238(G;G)
Reference rs727504238(A;A)
Significance Probable-Pathogenic
Disease not specified Familial hypertrophic cardiomyopathy 1 Hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN not specified Familial hypertrophic cardiomyopathy 1 Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23896955T>C
CLNSRC Centenary Institute
CLNACC RCV000154204.2, RCV000172889.1, RCV000226806.1,