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rs200303340

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200303340(C;T)
Make rs200303340(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415421
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs200303340
ebirs200303340
HLIrs200303340
Exacrs200303340
Varsomers200303340
Maprs200303340
PheGenIrs200303340
hapmaprs200303340
1000 genomesrs200303340
hgdprs200303340
ensemblrs200303340
gopubmedrs200303340
geneviewrs200303340
scholarrs200303340
googlers200303340
pharmgkbrs200303340
gwascentralrs200303340
openSNPrs200303340
23andMers200303340
23andMe allrs200303340
SNP Nexus

SNPshotrs200303340
SNPdbers200303340
MSV3drs200303340
GWAS Ctlgrs200303340
Max Magnitude0
ClinVar
Risk rs200303340(T;T)
Alt rs200303340(T;T)
Reference rs200303340(C;C)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not specified
Variation info
Gene MYH7 MHRT
CLNDBN Primary familial hypertrophic cardiomyopathy not specified
Reversed 0
HGVS NC_000014.8:g.23884630C>T
CLNSRC
CLNACC RCV000157365.1, RCV000158688.1,