rs527236059

Orientation

minus

Stabilized

minus

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

Make rs527236059(A;G)

Make rs527236059(G;G)

Reference

GRCh38 38.1/142

Chromosome

4

Position

47937505

Gene	CNGA1, LOC101927157

is a	snp
is	mentioned by
dbSNP	rs527236059
dbSNP (classic)	rs527236059
ClinGen	rs527236059
ebi	rs527236059
HLI	rs527236059
Exac	rs527236059
Gnomad	rs527236059
Varsome	rs527236059
LitVar	rs527236059
Map	rs527236059
PheGenI	rs527236059
Biobank	rs527236059
1000 genomes	rs527236059
hgdp	rs527236059
ensembl	rs527236059
geneview	rs527236059
scholar	rs527236059
google	rs527236059
pharmgkb	rs527236059
gwascentral	rs527236059
openSNP	rs527236059
23andMe	rs527236059
SNPshot	rs527236059
SNPdbe	rs527236059
MSV3d	rs527236059
GWAS Ctlg	rs527236059

Max Magnitude

0

ClinVar
Risk	rs527236059(G;G)
Alt	rs527236059(G;G)
Reference	Rs527236059(A;A)
Significance	Probable-Pathogenic
Disease	Retinitis pigmentosa
Variation	info
Gene	CNGA1 LOC101927157
CLNDBN	Retinitis pigmentosa
Reversed	1
HGVS	NC_000004.11:g.47939522T>C
CLNSRC	ClinVar
CLNACC	RCV000132618.1,