rs1057518927

Orientation

minus

Stabilized

minus

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

Make rs1057518927(A;G)

Make rs1057518927(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

124402952

Gene

OAT

is a	snp
is	mentioned by
dbSNP	rs1057518927
dbSNP (classic)	rs1057518927
ClinGen	rs1057518927
ebi	rs1057518927
HLI	rs1057518927
Exac	rs1057518927
Gnomad	rs1057518927
Varsome	rs1057518927
LitVar	rs1057518927
Map	rs1057518927
PheGenI	rs1057518927
Biobank	rs1057518927
1000 genomes	rs1057518927
hgdp	rs1057518927
ensembl	rs1057518927
geneview	rs1057518927
scholar	rs1057518927
google	rs1057518927
pharmgkb	rs1057518927
gwascentral	rs1057518927
openSNP	rs1057518927
23andMe	rs1057518927
SNPshot	rs1057518927
SNPdbe	rs1057518927
MSV3d	rs1057518927
GWAS Ctlg	rs1057518927

Max Magnitude

0

ClinVar
Risk	rs1057518927(G;G)
Alt	rs1057518927(G;G)
Reference	Rs1057518927(A;A)
Significance	Probable-Pathogenic
Disease	Abnormality of the choroid Optic atrophy Pain Visual field defect
Variation	info
Gene	OAT
CLNDBN	Abnormality of the choroid Optic atrophy Pain Visual field defect
Reversed	1
HGVS	NC_000010.10:g.126091521T>C
CLNSRC
CLNACC	RCV000415047.1,