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

rs56771886

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0
(T;T) 0 common in clinvar
Make rs56771886(-;-)
Make rs56771886(-;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156135923
GeneLMNA
is asnp
is mentioned by
dbSNPrs56771886
ebirs56771886
HLIrs56771886
Exacrs56771886
Varsomers56771886
Maprs56771886
PheGenIrs56771886
hapmaprs56771886
1000 genomesrs56771886
hgdprs56771886
ensemblrs56771886
gopubmedrs56771886
geneviewrs56771886
scholarrs56771886
googlers56771886
pharmgkbrs56771886
gwascentralrs56771886
openSNPrs56771886
23andMers56771886
23andMe allrs56771886
SNP Nexus

SNPshotrs56771886
SNPdbers56771886
MSV3drs56771886
GWAS Ctlgrs56771886
Max Magnitude0
ClinVar
Risk rs56771886(;)
Alt rs56771886(;)
Reference rs56771886(T;T)
Significance Pathogenic
Disease Dilated cardiomyopathy 1A Benign scapuloperoneal muscular dystrophy with cardiomyopathy not provided
Variation info
Gene LMNA
CLNDBN Dilated cardiomyopathy 1A Benign scapuloperoneal muscular dystrophy with cardiomyopathy not provided
Reversed 0
HGVS NC_000001.10:g.156105714delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000015581.22, RCV000015582.26, RCV000057492.1,