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

rs45544633

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45544633(C;T)
Make rs45544633(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23417174
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs45544633
ebirs45544633
HLIrs45544633
Exacrs45544633
Varsomers45544633
Maprs45544633
PheGenIrs45544633
hapmaprs45544633
1000 genomesrs45544633
hgdprs45544633
ensemblrs45544633
gopubmedrs45544633
geneviewrs45544633
scholarrs45544633
googlers45544633
pharmgkbrs45544633
gwascentralrs45544633
openSNPrs45544633
23andMers45544633
23andMe allrs45544633
SNP Nexus

SNPshotrs45544633
SNPdbers45544633
MSV3drs45544633
GWAS Ctlgrs45544633
Max Magnitude0
ClinVar
Risk rs45544633(T;T)
Alt rs45544633(T;T)
Reference rs45544633(C;C)
Significance Pathogenic
Disease Cardiomyopathy Hypertrophic cardiomyopathy
Variation info
Gene MYH7 MHRT
CLNDBN Cardiomyopathy Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23886383G>A
CLNSRC
CLNACC RCV000151238.2, RCV000232679.1,