rs1057517649

Orientation

minus

Stabilized

minus

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

Make rs1057517649(A;G)

Make rs1057517649(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

136677558

Gene

AGPAT2

is a	snp
is	mentioned by
dbSNP	rs1057517649
dbSNP (classic)	rs1057517649
ClinGen	rs1057517649
ebi	rs1057517649
HLI	rs1057517649
Exac	rs1057517649
Gnomad	rs1057517649
Varsome	rs1057517649
LitVar	rs1057517649
Map	rs1057517649
PheGenI	rs1057517649
Biobank	rs1057517649
1000 genomes	rs1057517649
hgdp	rs1057517649
ensembl	rs1057517649
geneview	rs1057517649
scholar	rs1057517649
google	rs1057517649
pharmgkb	rs1057517649
gwascentral	rs1057517649
openSNP	rs1057517649
23andMe	rs1057517649
SNPshot	rs1057517649
SNPdbe	rs1057517649
MSV3d	rs1057517649
GWAS Ctlg	rs1057517649

Max Magnitude

0

ClinVar
Risk	rs1057517649(G;G)
Alt	rs1057517649(G;G)
Reference	Rs1057517649(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.139572010T>C
CLNSRC
CLNACC	RCV000412588.1,