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rs193922712

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922712(A;G)
Make rs193922712(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position31821560
GeneMYLK2
is asnp
is mentioned by
dbSNPrs193922712
ebirs193922712
HLIrs193922712
Exacrs193922712
Varsomers193922712
Maprs193922712
PheGenIrs193922712
hapmaprs193922712
1000 genomesrs193922712
hgdprs193922712
ensemblrs193922712
gopubmedrs193922712
geneviewrs193922712
scholarrs193922712
googlers193922712
pharmgkbrs193922712
gwascentralrs193922712
openSNPrs193922712
23andMers193922712
23andMe allrs193922712
SNP Nexus

SNPshotrs193922712
SNPdbers193922712
MSV3drs193922712
GWAS Ctlgrs193922712
Max Magnitude0
ClinVar
Risk rs193922712(G;G)
Alt rs193922712(G;G)
Reference rs193922712(A;A)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYLK2
CLNDBN Cardiomyopathy
Reversed 0
HGVS NC_000020.10:g.30409363A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000030332.1,