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

rs61282106

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61282106(A;A)
Make rs61282106(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156136934
GeneLMNA
is asnp
is mentioned by
dbSNPrs61282106
ebirs61282106
HLIrs61282106
Exacrs61282106
Varsomers61282106
Maprs61282106
PheGenIrs61282106
hapmaprs61282106
1000 genomesrs61282106
hgdprs61282106
ensemblrs61282106
gopubmedrs61282106
geneviewrs61282106
scholarrs61282106
googlers61282106
pharmgkbrs61282106
gwascentralrs61282106
openSNPrs61282106
23andMers61282106
23andMe allrs61282106
SNP Nexus

SNPshotrs61282106
SNPdbers61282106
MSV3drs61282106
GWAS Ctlgrs61282106
Max Magnitude0
OMIM150330
Desc
Variant0015
Relatedalso


ClinVar
Risk rs61282106(A;A)
Alt rs61282106(A;A)
Reference rs61282106(G;G)
Significance Pathogenic
Disease Familial partial lipodystrophy 2 not provided
Variation info
Gene LMNA
CLNDBN Familial partial lipodystrophy 2 not provided
Reversed 0
HGVS NC_000001.10:g.156106725G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015584.26, RCV000057287.1,