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

rs369437262

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs369437262(C;C)
Make rs369437262(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415228
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs369437262
ebirs369437262
HLIrs369437262
Exacrs369437262
Varsomers369437262
Maprs369437262
PheGenIrs369437262
hapmaprs369437262
1000 genomesrs369437262
hgdprs369437262
ensemblrs369437262
gopubmedrs369437262
geneviewrs369437262
scholarrs369437262
googlers369437262
pharmgkbrs369437262
gwascentralrs369437262
openSNPrs369437262
23andMers369437262
23andMe allrs369437262
SNP Nexus

SNPshotrs369437262
SNPdbers369437262
MSV3drs369437262
GWAS Ctlgrs369437262
Max Magnitude0
ClinVar
Risk rs369437262(C;C)
Alt rs369437262(C;C)
Reference rs369437262(T;T)
Significance Probable-Pathogenic
Disease not specified Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH7 MHRT
CLNDBN not specified Familial hypertrophic cardiomyopathy 1
Reversed 0
HGVS NC_000014.8:g.23884437T>C
CLNSRC
CLNACC RCV000154209.1, RCV000168915.1,