rs2286455

Orientation

minus

Stabilized

minus

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

Make rs2286455(A;A)

Make rs2286455(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

16018539

Gene

PROM1

is a	snp
is	mentioned by
dbSNP	rs2286455
dbSNP (classic)	rs2286455
ClinGen	rs2286455
ebi	rs2286455
HLI	rs2286455
Exac	rs2286455
Gnomad	rs2286455
Varsome	rs2286455
LitVar	rs2286455
Map	rs2286455
PheGenI	rs2286455
Biobank	rs2286455
1000 genomes	rs2286455
hgdp	rs2286455
ensembl	rs2286455
geneview	rs2286455
scholar	rs2286455
google	rs2286455
pharmgkb	rs2286455
gwascentral	rs2286455
openSNP	rs2286455
23andMe	rs2286455
SNPshot	rs2286455
SNPdbe	rs2286455
MSV3d	rs2286455
GWAS Ctlg	rs2286455

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 26406410] Association of CD133 polymorphisms and response to bevacizumab in patients with metastatic colorectal cancer

ClinVar
Risk	rs2286455(A;A)
Alt	rs2286455(A;A)
Reference	Rs2286455(G;G)
Significance	Probable-non-pathogenic
Disease	not specified Cone-Rod Dystrophy Retinitis Pigmentosa Stargardt Disease Retinal Macular Dystrophy
Variation	info
Gene	PROM1
CLNDBN	not specified Cone-Rod Dystrophy, Dominant Retinitis Pigmentosa, Recessive Stargardt Disease, Dominant Retinal Macular Dystrophy
Reversed	1
HGVS	NC_000004.11:g.16020162C>T
CLNSRC
CLNACC	RCV000250373.1, RCV000279196.1, RCV000336486.1, RCV000375986.1, RCV000379416.1,