rs62638651

Orientation

minus

Stabilized

minus

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

Make rs62638651(C;T)

Make rs62638651(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38310690

Gene

RPGR

is a	snp
is	mentioned by
dbSNP	rs62638651
dbSNP (classic)	rs62638651
ClinGen	rs62638651
ebi	rs62638651
HLI	rs62638651
Exac	rs62638651
Gnomad	rs62638651
Varsome	rs62638651
LitVar	rs62638651
Map	rs62638651
PheGenI	rs62638651
Biobank	rs62638651
1000 genomes	rs62638651
hgdp	rs62638651
ensembl	rs62638651
geneview	rs62638651
scholar	rs62638651
google	rs62638651
pharmgkb	rs62638651
gwascentral	rs62638651
openSNP	rs62638651
23andMe	rs62638651
SNPshot	rs62638651
SNPdbe	rs62638651
MSV3d	rs62638651
GWAS Ctlg	rs62638651

Max Magnitude

0

OMIM	312610
Desc
Variant	0002
Related	also

ClinVar
Risk	rs62638651(T;T)
Alt	rs62638651(T;T)
Reference	Rs62638651(C;C)
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.38169943G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000010576.4, RCV000085116.1,