rs137852298

Orientation

minus

Stabilized

minus

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

Make rs137852298(C;T)

Make rs137852298(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

9760811

Gene

GPR143

is a	snp
is	mentioned by
dbSNP	rs137852298
dbSNP (classic)	rs137852298
ClinGen	rs137852298
ebi	rs137852298
HLI	rs137852298
Exac	rs137852298
Gnomad	rs137852298
Varsome	rs137852298
LitVar	rs137852298
Map	rs137852298
PheGenI	rs137852298
Biobank	rs137852298
1000 genomes	rs137852298
hgdp	rs137852298
ensembl	rs137852298
geneview	rs137852298
scholar	rs137852298
google	rs137852298
pharmgkb	rs137852298
gwascentral	rs137852298
openSNP	rs137852298
23andMe	rs137852298
SNPshot	rs137852298
SNPdbe	rs137852298
MSV3d	rs137852298
GWAS Ctlg	rs137852298

Max Magnitude

0

OMIM	300808
Desc
Variant	0009
Related	also

ClinVar
Risk	rs137852298(T;T)
Alt	rs137852298(T;T)
Reference	Rs137852298(C;C)
Significance	Pathogenic
Disease	Nystagmus 6
Variation	info
Gene	GPR143
CLNDBN	Nystagmus 6, congenital, X-linked
Reversed	1
HGVS	NC_000023.10:g.9728851G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000011268.7,