rs137852297

Orientation

minus

Stabilized

minus

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

Make rs137852297(A;A)

Make rs137852297(A;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

9743637

Gene

GPR143

is a	snp
is	mentioned by
dbSNP	rs137852297
dbSNP (classic)	rs137852297
ClinGen	rs137852297
ebi	rs137852297
HLI	rs137852297
Exac	rs137852297
Gnomad	rs137852297
Varsome	rs137852297
LitVar	rs137852297
Map	rs137852297
PheGenI	rs137852297
Biobank	rs137852297
1000 genomes	rs137852297
hgdp	rs137852297
ensembl	rs137852297
geneview	rs137852297
scholar	rs137852297
google	rs137852297
pharmgkb	rs137852297
gwascentral	rs137852297
openSNP	rs137852297
23andMe	rs137852297
SNPshot	rs137852297
SNPdbe	rs137852297
MSV3d	rs137852297
GWAS Ctlg	rs137852297

Merged from

Rs28935185

Max Magnitude

0

OMIM	300808
Desc
Variant	0005
Related	also

ClinVar
Risk	rs137852297(A;A) rs137852297(T;T)
Alt	rs137852297(A;A) rs137852297(T;T)
Reference	Rs137852297(C;C)
Significance	Pathogenic
Disease	Ocular albinism not provided
Variation	info
Gene	GPR143
CLNDBN	Ocular albinism, type I not provided
Reversed	1
HGVS	NC_000023.10:g.9711677G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000011264.5, RCV000084940.1,