rs727503796

Orientation

plus

Stabilized

plus

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

Make rs727503796(G;T)

Make rs727503796(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108141701

Gene

ACAT1

is a	snp
is	mentioned by
dbSNP	rs727503796
dbSNP (classic)	rs727503796
ClinGen	rs727503796
ebi	rs727503796
HLI	rs727503796
Exac	rs727503796
Gnomad	rs727503796
Varsome	rs727503796
LitVar	rs727503796
Map	rs727503796
PheGenI	rs727503796
Biobank	rs727503796
1000 genomes	rs727503796
hgdp	rs727503796
ensembl	rs727503796
geneview	rs727503796
scholar	rs727503796
google	rs727503796
pharmgkb	rs727503796
gwascentral	rs727503796
openSNP	rs727503796
23andMe	rs727503796
SNPshot	rs727503796
SNPdbe	rs727503796
MSV3d	rs727503796
GWAS Ctlg	rs727503796

Max Magnitude

0

ClinVar
Risk	rs727503796(T;T)
Alt	rs727503796(T;T)
Reference	Rs727503796(G;G)
Significance	Pathogenic
Disease	not provided Deficiency of acetyl-CoA acetyltransferase
Variation	info
Gene	ACAT1
CLNDBN	not provided Deficiency of acetyl-CoA acetyltransferase
Reversed	0
HGVS	NC_000011.9:g.108012428G>T
CLNSRC	HGMD
CLNACC	RCV000152744.2, RCV000180090.1,