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rs727504283

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504283(C;T)
Make rs727504283(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431804
GeneMYH7
is asnp
is mentioned by
dbSNPrs727504283
ebirs727504283
HLIrs727504283
Exacrs727504283
Varsomers727504283
Maprs727504283
PheGenIrs727504283
hapmaprs727504283
1000 genomesrs727504283
hgdprs727504283
ensemblrs727504283
gopubmedrs727504283
geneviewrs727504283
scholarrs727504283
googlers727504283
pharmgkbrs727504283
gwascentralrs727504283
openSNPrs727504283
23andMers727504283
23andMe allrs727504283
SNP Nexus

SNPshotrs727504283
SNPdbers727504283
MSV3drs727504283
GWAS Ctlgrs727504283
Max Magnitude0
ClinVar
Risk rs727504283(T;T)
Alt rs727504283(T;T)
Reference rs727504283(C;C)
Significance 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.23901013G>A
CLNSRC
CLNACC RCV000154292.2, RCV000158746.1,