rs104894093

Orientation

minus

Stabilized

minus

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

Make rs104894093(C;T)

Make rs104894093(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

136677537

Gene

AGPAT2

is a	snp
is	mentioned by
dbSNP	rs104894093
dbSNP (classic)	rs104894093
ClinGen	rs104894093
ebi	rs104894093
HLI	rs104894093
Exac	rs104894093
Gnomad	rs104894093
Varsome	rs104894093
LitVar	rs104894093
Map	rs104894093
PheGenI	rs104894093
Biobank	rs104894093
1000 genomes	rs104894093
hgdp	rs104894093
ensembl	rs104894093
geneview	rs104894093
scholar	rs104894093
google	rs104894093
pharmgkb	rs104894093
gwascentral	rs104894093
openSNP	rs104894093
23andMe	rs104894093
SNPshot	rs104894093
SNPdbe	rs104894093
MSV3d	rs104894093
GWAS Ctlg	rs104894093

Max Magnitude

0

OMIM	603100
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894093(T;T)
Alt	rs104894093(T;T)
Reference	Rs104894093(C;C)
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.139571989G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007003.3,