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rs267607591

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607591(A;A)
Make rs267607591(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position156135274
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607591
ebirs267607591
HLIrs267607591
Exacrs267607591
Varsomers267607591
Maprs267607591
PheGenIrs267607591
hapmaprs267607591
1000 genomesrs267607591
hgdprs267607591
ensemblrs267607591
gopubmedrs267607591
geneviewrs267607591
scholarrs267607591
googlers267607591
pharmgkbrs267607591
gwascentralrs267607591
openSNPrs267607591
23andMers267607591
23andMe allrs267607591
SNP Nexus

SNPshotrs267607591
SNPdbers267607591
MSV3drs267607591
GWAS Ctlgrs267607591
Max Magnitude0
ClinVar
Risk rs267607591(A;A)
Alt rs267607591(A;A)
Reference rs267607591(G;G)
Significance Probable-Pathogenic
Disease not provided Lipodystrophy
Variation info
Gene LMNA
CLNDBN not provided Lipodystrophy
Reversed 0
HGVS NC_000001.10:g.156105065G>A
CLNSRC ClinVar Epithelial Biology University of Chicago
CLNACC RCV000057481.1, RCV000146262.1,