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rs121908925

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908925(A;T)
Make rs121908925(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position136674753
GeneAGPAT2
is asnp
is mentioned by
dbSNPrs121908925
ebirs121908925
HLIrs121908925
Exacrs121908925
Varsomers121908925
Maprs121908925
PheGenIrs121908925
hapmaprs121908925
1000 genomesrs121908925
hgdprs121908925
ensemblrs121908925
gopubmedrs121908925
geneviewrs121908925
scholarrs121908925
googlers121908925
pharmgkbrs121908925
gwascentralrs121908925
openSNPrs121908925
23andMers121908925
23andMe allrs121908925
SNP Nexus

SNPshotrs121908925
SNPdbers121908925
MSV3drs121908925
GWAS Ctlgrs121908925
Max Magnitude0
OMIM603100
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121908925(T;T)
Alt rs121908925(T;T)
Reference rs121908925(A;A)
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.139569205T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007008.3,