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

rs121912497

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs121912497(A;A)
Make rs121912497(A;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position2435152
GeneLMNB2
is asnp
is mentioned by
dbSNPrs121912497
ebirs121912497
HLIrs121912497
Exacrs121912497
Varsomers121912497
Maprs121912497
PheGenIrs121912497
hapmaprs121912497
1000 genomesrs121912497
hgdprs121912497
ensemblrs121912497
gopubmedrs121912497
geneviewrs121912497
scholarrs121912497
googlers121912497
pharmgkbrs121912497
gwascentralrs121912497
openSNPrs121912497
23andMers121912497
23andMe allrs121912497
SNP Nexus

SNPshotrs121912497
SNPdbers121912497
MSV3drs121912497
GWAS Ctlgrs121912497
GMAF0.006887
Max Magnitude0
OMIM150341
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121912497(A;A)
Alt rs121912497(A;A)
Reference rs121912497(G;G)
Significance Other
Disease Acquired partial lipodystrophy not provided not specified
Variation info
Gene LMNB2 MIR7108
CLNDBN Acquired partial lipodystrophy not provided not specified
Reversed 1
HGVS NC_000019.9:g.2435150C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015561.2, RCV000057200.1, RCV000117496.2,