rs62638644

Orientation

minus

Stabilized

minus

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

Make rs62638644(G;G)

Make rs62638644(G;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38318909

Gene

RPGR

is a	snp
is	mentioned by
dbSNP	rs62638644
dbSNP (classic)	rs62638644
ClinGen	rs62638644
ebi	rs62638644
HLI	rs62638644
Exac	rs62638644
Gnomad	rs62638644
Varsome	rs62638644
LitVar	rs62638644
Map	rs62638644
PheGenI	rs62638644
Biobank	rs62638644
1000 genomes	rs62638644
hgdp	rs62638644
ensembl	rs62638644
geneview	rs62638644
scholar	rs62638644
google	rs62638644
pharmgkb	rs62638644
gwascentral	rs62638644
openSNP	rs62638644
23andMe	rs62638644
SNPshot	rs62638644
SNPdbe	rs62638644
MSV3d	rs62638644
GWAS Ctlg	rs62638644

Max Magnitude

0

OMIM	312610
Desc
Variant	0001
Related	also

ClinVar
Risk	rs62638644(G;G)
Alt	rs62638644(G;G)
Reference	Rs62638644(T;T)
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.38178162A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000010575.2, RCV000085105.1,