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rs193922391

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922391(A;G)
Make rs193922391(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position46858413
GeneMYL3
is asnp
is mentioned by
dbSNPrs193922391
ebirs193922391
HLIrs193922391
Exacrs193922391
Varsomers193922391
Maprs193922391
PheGenIrs193922391
hapmaprs193922391
1000 genomesrs193922391
hgdprs193922391
ensemblrs193922391
gopubmedrs193922391
geneviewrs193922391
scholarrs193922391
googlers193922391
pharmgkbrs193922391
gwascentralrs193922391
openSNPrs193922391
23andMers193922391
23andMe allrs193922391
SNP Nexus

SNPshotrs193922391
SNPdbers193922391
MSV3drs193922391
GWAS Ctlgrs193922391
Max Magnitude0
ClinVar
Risk rs193922391(G;G)
Alt rs193922391(G;G)
Reference rs193922391(A;A)
Significance Other
Disease Primary familial hypertrophic cardiomyopathy not specified
Variation info
Gene MYL3
CLNDBN Primary familial hypertrophic cardiomyopathy not specified
Reversed 1
HGVS NC_000003.11:g.46899903T>C
CLNSRC ClinVar LabCorp University of Washington
CLNACC RCV000030327.3, RCV000223754.2,