rs121965034

Orientation

minus

Stabilized

minus

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

Make rs121965034(A;A)

Make rs121965034(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

124412169

Gene

OAT

is a	snp
is	mentioned by
dbSNP	rs121965034
dbSNP (classic)	rs121965034
ClinGen	rs121965034
ebi	rs121965034
HLI	rs121965034
Exac	rs121965034
Gnomad	rs121965034
Varsome	rs121965034
LitVar	rs121965034
Map	rs121965034
PheGenI	rs121965034
Biobank	rs121965034
1000 genomes	rs121965034
hgdp	rs121965034
ensembl	rs121965034
geneview	rs121965034
scholar	rs121965034
google	rs121965034
pharmgkb	rs121965034
gwascentral	rs121965034
openSNP	rs121965034
23andMe	rs121965034
SNPshot	rs121965034
SNPdbe	rs121965034
MSV3d	rs121965034
GWAS Ctlg	rs121965034

Max Magnitude

0

OMIM	613349
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121965034(A;A)
Alt	rs121965034(A;A)
Reference	Rs121965034(G;G)
Significance	Pathogenic
Disease	Ornithine aminotransferase deficiency
Variation	info
Gene	OAT
CLNDBN	Ornithine aminotransferase deficiency
Reversed	1
HGVS	NC_000010.10:g.126100738C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000169.3,