rs62642057

Orientation

minus

Stabilized

minus

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

Make rs62642057(A;A)

Make rs62642057(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38304746

Gene

RPGR

is a	snp
is	mentioned by
dbSNP	rs62642057
dbSNP (classic)	rs62642057
ClinGen	rs62642057
ebi	rs62642057
HLI	rs62642057
Exac	rs62642057
Gnomad	rs62642057
Varsome	rs62642057
LitVar	rs62642057
Map	rs62642057
PheGenI	rs62642057
Biobank	rs62642057
1000 genomes	rs62642057
hgdp	rs62642057
ensembl	rs62642057
geneview	rs62642057
scholar	rs62642057
google	rs62642057
pharmgkb	rs62642057
gwascentral	rs62642057
openSNP	rs62642057
23andMe	rs62642057
SNPshot	rs62642057
SNPdbe	rs62642057
MSV3d	rs62642057
GWAS Ctlg	rs62642057

Max Magnitude

0

OMIM	312610
Desc
Variant	0003
Related	also

ClinVar
Risk	rs62642057(A;A)
Alt	rs62642057(A;A)
Reference	Rs62642057(G;G)
Significance	Pathogenic
Disease	Retinitis pigmentosa 15 not provided
Variation	info
Gene	RPGR
CLNDBN	Retinitis pigmentosa 15 not provided
Reversed	1
HGVS	NC_000023.10:g.38163999C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000010577.5, RCV000085125.1,