rs62638634

Orientation

minus

Stabilized

minus

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

Make rs62638634(G;T)

Make rs62638634(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38322921

Gene

RPGR

is a	snp
is	mentioned by
dbSNP	rs62638634
dbSNP (classic)	rs62638634
ClinGen	rs62638634
ebi	rs62638634
HLI	rs62638634
Exac	rs62638634
Gnomad	rs62638634
Varsome	rs62638634
LitVar	rs62638634
Map	rs62638634
PheGenI	rs62638634
Biobank	rs62638634
1000 genomes	rs62638634
hgdp	rs62638634
ensembl	rs62638634
geneview	rs62638634
scholar	rs62638634
google	rs62638634
pharmgkb	rs62638634
gwascentral	rs62638634
openSNP	rs62638634
23andMe	rs62638634
SNPshot	rs62638634
SNPdbe	rs62638634
MSV3d	rs62638634
GWAS Ctlg	rs62638634

Max Magnitude

0

OMIM	312610
Desc
Variant	0006
Related	also

ClinVar
Risk	rs62638634(T;T)
Alt	rs62638634(T;T)
Reference	Rs62638634(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.38182174C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000010580.4, RCV000085072.1,