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

rs59026483

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs59026483(C;T)
Make rs59026483(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156134457
GeneLMNA
is asnp
is mentioned by
dbSNPrs59026483
ebirs59026483
HLIrs59026483
Exacrs59026483
Varsomers59026483
Maprs59026483
PheGenIrs59026483
hapmaprs59026483
1000 genomesrs59026483
hgdprs59026483
ensemblrs59026483
gopubmedrs59026483
geneviewrs59026483
scholarrs59026483
googlers59026483
pharmgkbrs59026483
gwascentralrs59026483
openSNPrs59026483
23andMers59026483
23andMe allrs59026483
SNP Nexus

SNPshotrs59026483
SNPdbers59026483
MSV3drs59026483
GWAS Ctlgrs59026483
Max Magnitude0
ClinVar
Risk rs59026483(T;T)
Alt rs59026483(T;T)
Reference rs59026483(C;C)
Significance Pathogenic
Disease not provided Dilated cardiomyopathy 1A
Variation info
Gene LMNA
CLNDBN not provided Dilated cardiomyopathy 1A
Reversed 0
HGVS NC_000001.10:g.156104248C>T
CLNSRC
CLNACC RCV000057419.3, RCV000177232.1,