rs104894926

Orientation

plus

Stabilized

plus

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

Make rs104894926(C;G)

Make rs104894926(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

46853826

Gene

RP2

is a	snp
is	mentioned by
dbSNP	rs104894926
dbSNP (classic)	rs104894926
ClinGen	rs104894926
ebi	rs104894926
HLI	rs104894926
Exac	rs104894926
Gnomad	rs104894926
Varsome	rs104894926
LitVar	rs104894926
Map	rs104894926
PheGenI	rs104894926
Biobank	rs104894926
1000 genomes	rs104894926
hgdp	rs104894926
ensembl	rs104894926
geneview	rs104894926
scholar	rs104894926
google	rs104894926
pharmgkb	rs104894926
gwascentral	rs104894926
openSNP	rs104894926
23andMe	rs104894926
SNPshot	rs104894926
SNPdbe	rs104894926
MSV3d	rs104894926
GWAS Ctlg	rs104894926

Max Magnitude

0

OMIM	300757
Desc
Variant	0004
Related	also

ClinVar
Risk	rs104894926(G;G)
Alt	rs104894926(G;G)
Reference	Rs104894926(C;C)
Significance	Pathogenic
Disease	Retinitis pigmentosa 2
Variation	info
Gene	RP2
CLNDBN	Retinitis pigmentosa 2
Reversed	0
HGVS	NC_000023.10:g.46713261C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011293.2,