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rs375667565

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs375667565(A;A)
Make rs375667565(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position110913124
GeneMYL2
is asnp
is mentioned by
dbSNPrs375667565
ebirs375667565
HLIrs375667565
Exacrs375667565
Varsomers375667565
Maprs375667565
PheGenIrs375667565
hapmaprs375667565
1000 genomesrs375667565
hgdprs375667565
ensemblrs375667565
gopubmedrs375667565
geneviewrs375667565
scholarrs375667565
googlers375667565
pharmgkbrs375667565
gwascentralrs375667565
openSNPrs375667565
23andMers375667565
23andMe allrs375667565
SNP Nexus

SNPshotrs375667565
SNPdbers375667565
MSV3drs375667565
GWAS Ctlgrs375667565
Max Magnitude0
ClinVar
Risk rs375667565(A;A)
Alt rs375667565(A;A)
Reference rs375667565(G;G)
Significance Probable-Pathogenic
Disease not specified Cardiomyopathy not provided
Variation info
Gene MYL2
CLNDBN not specified Cardiomyopathy not provided
Reversed 0
HGVS NC_000012.11:g.111350928G>A
CLNSRC
CLNACC RCV000036400.2, RCV000157370.2, RCV000158930.1,