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rs863225024

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225024(-;G)
Make rs863225024(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156138750
GeneLMNA
is asnp
is mentioned by
dbSNPrs863225024
dbSNP (old)rs863225024
ClinGenrs863225024
ebirs863225024
HLIrs863225024
Exacrs863225024
Gnomadrs863225024
Varsomers863225024
Maprs863225024
PheGenIrs863225024
Biobankrs863225024
1000 genomesrs863225024
hgdprs863225024
ensemblrs863225024
gopubmedrs863225024
geneviewrs863225024
scholarrs863225024
googlers863225024
pharmgkbrs863225024
gwascentralrs863225024
openSNPrs863225024
23andMers863225024
23andMe allrs863225024
SNP Nexus

SNPshotrs863225024
SNPdbers863225024
MSV3drs863225024
GWAS Ctlgrs863225024
Max Magnitude0
ClinVar
Risk rs863225024(G;G)
Alt rs863225024(G;G)
Reference Rs863225024(-;-)
Significance Pathogenic
Disease not provided Familial partial lipodystrophy 2
Variation info
Gene LMNA
CLNDBN not provided Familial partial lipodystrophy 2
Reversed 0
HGVS NC_000001.10:g.156108541dupG
CLNSRC Quest Diagnostics
CLNACC RCV000057376.1, RCV000201023.1,