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rs369940645

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369940645(C;T)
Make rs369940645(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23415132
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs369940645
ebirs369940645
HLIrs369940645
Exacrs369940645
Varsomers369940645
Maprs369940645
PheGenIrs369940645
hapmaprs369940645
1000 genomesrs369940645
hgdprs369940645
ensemblrs369940645
gopubmedrs369940645
geneviewrs369940645
scholarrs369940645
googlers369940645
pharmgkbrs369940645
gwascentralrs369940645
openSNPrs369940645
23andMers369940645
23andMe allrs369940645
SNP Nexus

SNPshotrs369940645
SNPdbers369940645
MSV3drs369940645
GWAS Ctlgrs369940645
Max Magnitude0
ClinVar
Risk rs369940645(T;T)
Alt rs369940645(T;T)
Reference rs369940645(C;C)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH7 MHRT
CLNDBN Familial hypertrophic cardiomyopathy 1
Reversed 0
HGVS NC_000014.8:g.23884341C>T
CLNSRC
CLNACC RCV000201453.1,