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rs111569862

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111569862(C;C)
Make rs111569862(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156137653
GeneLMNA
is asnp
is mentioned by
dbSNPrs111569862
ebirs111569862
HLIrs111569862
Exacrs111569862
Varsomers111569862
Maprs111569862
PheGenIrs111569862
hapmaprs111569862
1000 genomesrs111569862
hgdprs111569862
ensemblrs111569862
gopubmedrs111569862
geneviewrs111569862
scholarrs111569862
googlers111569862
pharmgkbrs111569862
gwascentralrs111569862
openSNPrs111569862
23andMers111569862
23andMe allrs111569862
SNP Nexus

SNPshotrs111569862
SNPdbers111569862
MSV3drs111569862
GWAS Ctlgrs111569862
Max Magnitude0
ClinVar
Risk rs111569862(A,C;A,C)
Alt rs111569862(A,C;A,C)
Reference rs111569862(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.156107444G>A
CLNSRC
CLNACC RCV000156608.1, RCV000182373.1,