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

rs121908926

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908926(A;A)
Make rs121908926(A;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position136676603
GeneAGPAT2
is asnp
is mentioned by
dbSNPrs121908926
ebirs121908926
HLIrs121908926
Exacrs121908926
Varsomers121908926
Maprs121908926
PheGenIrs121908926
hapmaprs121908926
1000 genomesrs121908926
hgdprs121908926
ensemblrs121908926
gopubmedrs121908926
geneviewrs121908926
scholarrs121908926
googlers121908926
pharmgkbrs121908926
gwascentralrs121908926
openSNPrs121908926
23andMers121908926
23andMe allrs121908926
SNP Nexus

SNPshotrs121908926
SNPdbers121908926
MSV3drs121908926
GWAS Ctlgrs121908926
Max Magnitude0
OMIM603100
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121908926(A,T;A,T)
Alt rs121908926(A,T;A,T)
Reference rs121908926(C;C)
Significance Pathogenic
Disease Congenital generalized lipodystrophy type 1
Variation info
Gene AGPAT2
CLNDBN Congenital generalized lipodystrophy type 1
Reversed 1
HGVS NC_000009.11:g.139571055G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007010.3,