rs387906355

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Make rs387906355(-;T)

Make rs387906355(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

136677075

Gene

AGPAT2

is a	snp
is	mentioned by
dbSNP	rs387906355
dbSNP (classic)	rs387906355
ClinGen	rs387906355
ebi	rs387906355
HLI	rs387906355
Exac	rs387906355
Gnomad	rs387906355
Varsome	rs387906355
LitVar	rs387906355
Map	rs387906355
PheGenI	rs387906355
Biobank	rs387906355
1000 genomes	rs387906355
hgdp	rs387906355
ensembl	rs387906355
geneview	rs387906355
scholar	rs387906355
google	rs387906355
pharmgkb	rs387906355
gwascentral	rs387906355
openSNP	rs387906355
23andMe	rs387906355
SNPshot	rs387906355
SNPdbe	rs387906355
MSV3d	rs387906355
GWAS Ctlg	rs387906355

Max Magnitude

0

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,