rs62638632

Orientation

minus

Stabilized

minus

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

Make rs62638632(A;G)

Make rs62638632(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38322947

Gene

RPGR

is a	snp
is	mentioned by
dbSNP	rs62638632
dbSNP (classic)	rs62638632
ClinGen	rs62638632
ebi	rs62638632
HLI	rs62638632
Exac	rs62638632
Gnomad	rs62638632
Varsome	rs62638632
LitVar	rs62638632
Map	rs62638632
PheGenI	rs62638632
Biobank	rs62638632
1000 genomes	rs62638632
hgdp	rs62638632
ensembl	rs62638632
geneview	rs62638632
scholar	rs62638632
google	rs62638632
pharmgkb	rs62638632
gwascentral	rs62638632
openSNP	rs62638632
23andMe	rs62638632
SNPshot	rs62638632
SNPdbe	rs62638632
MSV3d	rs62638632
GWAS Ctlg	rs62638632

Max Magnitude

0

ClinVar
Risk	rs62638632(G;G)
Alt	rs62638632(G;G)
Reference	Rs62638632(A;A)
Significance	Pathogenic
Disease	not provided Retinitis pigmentosa 15
Variation	info
Gene	RPGR
CLNDBN	not provided Retinitis pigmentosa 15
Reversed	1
HGVS	NC_000023.10:g.38182200T>C
CLNSRC	HGMD
CLNACC	RCV000078647.4, RCV000177041.1,