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rs727504320

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727504320(A;A)
Make rs727504320(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23425735
GeneMYH7
is asnp
is mentioned by
dbSNPrs727504320
ebirs727504320
HLIrs727504320
Exacrs727504320
Varsomers727504320
Maprs727504320
PheGenIrs727504320
hapmaprs727504320
1000 genomesrs727504320
hgdprs727504320
ensemblrs727504320
gopubmedrs727504320
geneviewrs727504320
scholarrs727504320
googlers727504320
pharmgkbrs727504320
gwascentralrs727504320
openSNPrs727504320
23andMers727504320
23andMe allrs727504320
SNP Nexus

SNPshotrs727504320
SNPdbers727504320
MSV3drs727504320
GWAS Ctlgrs727504320
Max Magnitude0
ClinVar
Risk rs727504320(A;A)
Alt rs727504320(A;A)
Reference rs727504320(T;T)
Significance Probable-Pathogenic
Disease not specified Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH7
CLNDBN not specified Familial hypertrophic cardiomyopathy 1
Reversed 1
HGVS NC_000014.8:g.23894944A>T
CLNSRC
CLNACC RCV000154410.2, RCV000168867.1,