rs527236062

Orientation

plus

Stabilized

plus

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

Make rs527236062(C;C)

Make rs527236062(C;G)

Reference

GRCh38 38.1/142

Chromosome

19

Position

47836335

Gene

CRX

is a	snp
is	mentioned by
dbSNP	rs527236062
dbSNP (classic)	rs527236062
ClinGen	rs527236062
ebi	rs527236062
HLI	rs527236062
Exac	rs527236062
Gnomad	rs527236062
Varsome	rs527236062
LitVar	rs527236062
Map	rs527236062
PheGenI	rs527236062
Biobank	rs527236062
1000 genomes	rs527236062
hgdp	rs527236062
ensembl	rs527236062
geneview	rs527236062
scholar	rs527236062
google	rs527236062
pharmgkb	rs527236062
gwascentral	rs527236062
openSNP	rs527236062
23andMe	rs527236062
SNPshot	rs527236062
SNPdbe	rs527236062
MSV3d	rs527236062
GWAS Ctlg	rs527236062

Max Magnitude

0

ClinVar
Risk	rs527236062(C;C)
Alt	rs527236062(C;C)
Reference	Rs527236062(G;G)
Significance	Pathogenic
Disease	Retinitis pigmentosa
Variation	info
Gene	CRX
CLNDBN	Retinitis pigmentosa
Reversed	0
HGVS	NC_000019.9:g.48339592G>C
CLNSRC	ClinVar
CLNACC	RCV000132604.1,