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rs553016

From SNPedia

Orientationminus
Stabilizedminus
Make rs553016(A;A)
Make rs553016(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156137072
GeneLMNA
is asnp
is mentioned by
dbSNPrs553016
ebirs553016
HLIrs553016
Exacrs553016
Varsomers553016
Maprs553016
PheGenIrs553016
hapmaprs553016
1000 genomesrs553016
hgdprs553016
ensemblrs553016
gopubmedrs553016
geneviewrs553016
scholarrs553016
googlers553016
pharmgkbrs553016
gwascentralrs553016
openSNPrs553016
23andMers553016
23andMe allrs553016
SNP Nexus

SNPshotrs553016
SNPdbers553016
MSV3drs553016
GWAS Ctlgrs553016
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 24831476] [Association between LMNA mutation and familial and idiopathic dilated cardiomyopathy patients in Xinjiang]


ClinVar
Risk rs553016(A;A)
Alt rs553016(A;A)
Reference rs553016(G;G)
Significance Untested
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.156106863C>T
CLNSRC ClinVar Epithelial Biology
CLNACC RCV000057308.1,