rs267606924

Orientation

minus

Stabilized

minus

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

Make rs267606924(A;A)

Make rs267606924(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

124403003

Gene

OAT

is a	snp
is	mentioned by
dbSNP	rs267606924
dbSNP (classic)	rs267606924
ClinGen	rs267606924
ebi	rs267606924
HLI	rs267606924
Exac	rs267606924
Gnomad	rs267606924
Varsome	rs267606924
LitVar	rs267606924
Map	rs267606924
PheGenI	rs267606924
Biobank	rs267606924
1000 genomes	rs267606924
hgdp	rs267606924
ensembl	rs267606924
geneview	rs267606924
scholar	rs267606924
google	rs267606924
pharmgkb	rs267606924
gwascentral	rs267606924
openSNP	rs267606924
23andMe	rs267606924
SNPshot	rs267606924
SNPdbe	rs267606924
MSV3d	rs267606924
GWAS Ctlg	rs267606924

Max Magnitude

0

ClinVar
Risk	rs267606924(A;A)
Alt	rs267606924(A;A)
Reference	Rs267606924(G;G)
Significance	Pathogenic
Disease	Ornithine aminotransferase deficiency
Variation	info
Gene	OAT
CLNDBN	Ornithine aminotransferase deficiency
Reversed	1
HGVS	NC_000010.10:g.126091572C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000203.2,