rs1057517652

Orientation

minus

Stabilized

minus

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

Make rs1057517652(A;A)

Make rs1057517652(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

136676960

Gene

AGPAT2

is a	snp
is	mentioned by
dbSNP	rs1057517652
dbSNP (classic)	rs1057517652
ClinGen	rs1057517652
ebi	rs1057517652
HLI	rs1057517652
Exac	rs1057517652
Gnomad	rs1057517652
Varsome	rs1057517652
LitVar	rs1057517652
Map	rs1057517652
PheGenI	rs1057517652
Biobank	rs1057517652
1000 genomes	rs1057517652
hgdp	rs1057517652
ensembl	rs1057517652
geneview	rs1057517652
scholar	rs1057517652
google	rs1057517652
pharmgkb	rs1057517652
gwascentral	rs1057517652
openSNP	rs1057517652
23andMe	rs1057517652
SNPshot	rs1057517652
SNPdbe	rs1057517652
MSV3d	rs1057517652
GWAS Ctlg	rs1057517652

Max Magnitude

0

ClinVar
Risk	rs1057517652(A;A)
Alt	rs1057517652(A;A)
Reference	Rs1057517652(G;G)
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.139571412C>T
CLNSRC
CLNACC	RCV000412609.1,