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rs387906355

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs387906355(-;-)
Make rs387906355(-;T)
Make rs387906355(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position136677075
GeneAGPAT2
is asnp
is mentioned by
dbSNPrs387906355
ebirs387906355
HLIrs387906355
Exacrs387906355
Varsomers387906355
Maprs387906355
PheGenIrs387906355
hapmaprs387906355
1000 genomesrs387906355
hgdprs387906355
ensemblrs387906355
gopubmedrs387906355
geneviewrs387906355
scholarrs387906355
googlers387906355
pharmgkbrs387906355
gwascentralrs387906355
openSNPrs387906355
23andMers387906355
23andMe allrs387906355
SNP Nexus

SNPshotrs387906355
SNPdbers387906355
MSV3drs387906355
GWAS Ctlgrs387906355
Max Magnitude0
ClinVar
Risk rs387906355(T;T)
Alt rs387906355(T;T)
Reference rs387906355(;)
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.139571528dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000007005.3,