rs11461

Orientation

minus

Stabilized

minus

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

Make rs11461(C;T)

Make rs11461(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

124400865

Gene

OAT

is a	snp
is	mentioned by
dbSNP	rs11461
dbSNP (classic)	rs11461
ClinGen	rs11461
ebi	rs11461
HLI	rs11461
Exac	rs11461
Gnomad	rs11461
Varsome	rs11461
LitVar	rs11461
Map	rs11461
PheGenI	rs11461
Biobank	rs11461
1000 genomes	rs11461
hgdp	rs11461
ensembl	rs11461
geneview	rs11461
scholar	rs11461
google	rs11461
pharmgkb	rs11461
gwascentral	rs11461
openSNP	rs11461
23andMe	rs11461
SNPshot	rs11461
SNPdbe	rs11461
MSV3d	rs11461
GWAS Ctlg	rs11461

GMAF

0.4109

Max Magnitude

0

OMIM	258870
Desc	OAT POLYMORPHISM
Variant	0017
Related	also

OMIM	613349
Desc
Variant	0017
Related	also

ClinVar
Risk	rs11461(T;T)
Alt	rs11461(T;T)
Reference	Rs11461(C;C)
Significance	Non-pathogenic
Disease	OAT POLYMORPHISM Ornithine aminotransferase deficiency
Variation	info
Gene	OAT
CLNDBN	OAT POLYMORPHISM Ornithine aminotransferase deficiency
Reversed	1
HGVS	NC_000010.10:g.126089434G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000184.2, RCV000380778.1,