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rs373514686

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs373514686(C;T)
Make rs373514686(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23416140
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs373514686
ebirs373514686
HLIrs373514686
Exacrs373514686
Varsomers373514686
Maprs373514686
PheGenIrs373514686
hapmaprs373514686
1000 genomesrs373514686
hgdprs373514686
ensemblrs373514686
gopubmedrs373514686
geneviewrs373514686
scholarrs373514686
googlers373514686
pharmgkbrs373514686
gwascentralrs373514686
openSNPrs373514686
23andMers373514686
23andMe allrs373514686
SNP Nexus

SNPshotrs373514686
SNPdbers373514686
MSV3drs373514686
GWAS Ctlgrs373514686
Max Magnitude0
ClinVar
Risk rs373514686(T;T)
Alt rs373514686(T;T)
Reference rs373514686(C;C)
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.23885349C>T
CLNSRC
CLNACC RCV000035933.3, RCV000201450.1,