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

rs59981161

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs59981161(C;C)
Make rs59981161(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156136998
GeneLMNA
is asnp
is mentioned by
dbSNPrs59981161
ebirs59981161
HLIrs59981161
Exacrs59981161
Varsomers59981161
Maprs59981161
PheGenIrs59981161
hapmaprs59981161
1000 genomesrs59981161
hgdprs59981161
ensemblrs59981161
gopubmedrs59981161
geneviewrs59981161
scholarrs59981161
googlers59981161
pharmgkbrs59981161
gwascentralrs59981161
openSNPrs59981161
23andMers59981161
23andMe allrs59981161
SNP Nexus

SNPshotrs59981161
SNPdbers59981161
MSV3drs59981161
GWAS Ctlgrs59981161
Max Magnitude0
ClinVar
Risk rs59981161(C,T;C,T)
Alt rs59981161(C,T;C,T)
Reference rs59981161(G;G)
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.156106789G>C; NC_000001.10:g.156106789G>T
CLNSRC
CLNACC RCV000057301.1, RCV000057302.1, RCV000193901.1,