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rs387906356

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TTC;TTC) 0 common in clinvar
Make rs387906356(-;-)
Make rs387906356(-;TTC)
ReferenceGRCh38 38.1/141
Chromosome9
Position136677033
GeneAGPAT2
is asnp
is mentioned by
dbSNPrs387906356
ebirs387906356
HLIrs387906356
Exacrs387906356
Varsomers387906356
Maprs387906356
PheGenIrs387906356
hapmaprs387906356
1000 genomesrs387906356
hgdprs387906356
ensemblrs387906356
gopubmedrs387906356
geneviewrs387906356
scholarrs387906356
googlers387906356
pharmgkbrs387906356
gwascentralrs387906356
openSNPrs387906356
23andMers387906356
23andMe allrs387906356
SNP Nexus

SNPshotrs387906356
SNPdbers387906356
MSV3drs387906356
GWAS Ctlgrs387906356
Max Magnitude0
ClinVar
Risk rs387906356(;)
Alt rs387906356(;)
Reference rs387906356(TTC;TTC)
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.139571485_139571487delGAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000007007.3,