Have questions? Visit https://www.reddit.com/r/SNPedia

rs727505202

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727505202(C;C)
Make rs727505202(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23431459
GeneMYH7
is asnp
is mentioned by
dbSNPrs727505202
ebirs727505202
HLIrs727505202
Exacrs727505202
Varsomers727505202
Maprs727505202
PheGenIrs727505202
hapmaprs727505202
1000 genomesrs727505202
hgdprs727505202
ensemblrs727505202
gopubmedrs727505202
geneviewrs727505202
scholarrs727505202
googlers727505202
pharmgkbrs727505202
gwascentralrs727505202
openSNPrs727505202
23andMers727505202
23andMe allrs727505202
SNP Nexus

SNPshotrs727505202
SNPdbers727505202
MSV3drs727505202
GWAS Ctlgrs727505202
Max Magnitude0
ClinVar
Risk rs727505202(C;C)
Alt rs727505202(C;C)
Reference rs727505202(T;T)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 1 not specified
Variation info
Gene MYH7
CLNDBN Familial hypertrophic cardiomyopathy 1 not specified
Reversed 1
HGVS NC_000014.8:g.23900668A>C; NC_000014.8:g.23900668A>G
CLNSRC
CLNACC RCV000201463.1, RCV000156695.1,