rs527236057

Orientation

minus

Stabilized

minus

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

Make rs527236057(A;A)

Make rs527236057(A;G)

Reference

GRCh38 38.1/142

Chromosome

4

Position

47936861

Gene	CNGA1, LOC101927157

is a	snp
is	mentioned by
dbSNP	rs527236057
dbSNP (classic)	rs527236057
ClinGen	rs527236057
ebi	rs527236057
HLI	rs527236057
Exac	rs527236057
Gnomad	rs527236057
Varsome	rs527236057
LitVar	rs527236057
Map	rs527236057
PheGenI	rs527236057
Biobank	rs527236057
1000 genomes	rs527236057
hgdp	rs527236057
ensembl	rs527236057
geneview	rs527236057
scholar	rs527236057
google	rs527236057
pharmgkb	rs527236057
gwascentral	rs527236057
openSNP	rs527236057
23andMe	rs527236057
SNPshot	rs527236057
SNPdbe	rs527236057
MSV3d	rs527236057
GWAS Ctlg	rs527236057

Max Magnitude

0

ClinVar
Risk	rs527236057(A;A)
Alt	rs527236057(A;A)
Reference	Rs527236057(G;G)
Significance	Probable-Pathogenic
Disease	Retinitis pigmentosa
Variation	info
Gene	CNGA1 LOC101927157
CLNDBN	Retinitis pigmentosa
Reversed	1
HGVS	NC_000004.11:g.47938878C>T
CLNSRC	ClinVar
CLNACC	RCV000132619.1,