rs267606923

Orientation

minus

Stabilized

minus

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

Make rs267606923(A;A)

Make rs267606923(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

124405551

Gene

OAT

is a	snp
is	mentioned by
dbSNP	rs267606923
dbSNP (classic)	rs267606923
ClinGen	rs267606923
ebi	rs267606923
HLI	rs267606923
Exac	rs267606923
Gnomad	rs267606923
Varsome	rs267606923
LitVar	rs267606923
Map	rs267606923
PheGenI	rs267606923
Biobank	rs267606923
1000 genomes	rs267606923
hgdp	rs267606923
ensembl	rs267606923
geneview	rs267606923
scholar	rs267606923
google	rs267606923
pharmgkb	rs267606923
gwascentral	rs267606923
openSNP	rs267606923
23andMe	rs267606923
SNPshot	rs267606923
SNPdbe	rs267606923
MSV3d	rs267606923
GWAS Ctlg	rs267606923

Max Magnitude

0

ClinVar
Risk	rs267606923(A;A)
Alt	rs267606923(A;A)
Reference	Rs267606923(G;G)
Significance	Pathogenic
Disease	Ornithine aminotransferase deficiency
Variation	info
Gene	OAT
CLNDBN	Ornithine aminotransferase deficiency
Reversed	1
HGVS	NC_000010.10:g.126094120C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000202.2,