Have questions? Visit https://www.reddit.com/r/SNPedia

rs56816490

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs56816490(A;A)
Make rs56816490(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156135913
GeneLMNA
is asnp
is mentioned by
dbSNPrs56816490
ebirs56816490
HLIrs56816490
Exacrs56816490
Varsomers56816490
Maprs56816490
PheGenIrs56816490
hapmaprs56816490
1000 genomesrs56816490
hgdprs56816490
ensemblrs56816490
gopubmedrs56816490
geneviewrs56816490
scholarrs56816490
googlers56816490
pharmgkbrs56816490
gwascentralrs56816490
openSNPrs56816490
23andMers56816490
23andMe allrs56816490
SNP Nexus

SNPshotrs56816490
SNPdbers56816490
MSV3drs56816490
GWAS Ctlgrs56816490
Max Magnitude0
ClinVar
Risk rs56816490(A,T;A,T)
Alt rs56816490(A,T;A,T)
Reference rs56816490(G;G)
Significance Pathogenic
Disease Primary dilated cardiomyopathy not provided
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy not provided
Reversed 0
HGVS NC_000001.10:g.156105704G>A; NC_000001.10:g.156105704G>T
CLNSRC ClinVar Epithelial Biology
CLNACC RCV000041379.2, RCV000057489.2, RCV000223858.1,