rs527236060

Orientation

minus

Stabilized

minus

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

Make rs527236060(C;C)

Make rs527236060(C;G)

Reference

GRCh38 38.1/142

Chromosome

16

Position

57964482

Gene

CNGB1

is a	snp
is	mentioned by
dbSNP	rs527236060
dbSNP (classic)	rs527236060
ClinGen	rs527236060
ebi	rs527236060
HLI	rs527236060
Exac	rs527236060
Gnomad	rs527236060
Varsome	rs527236060
LitVar	rs527236060
Map	rs527236060
PheGenI	rs527236060
Biobank	rs527236060
1000 genomes	rs527236060
hgdp	rs527236060
ensembl	rs527236060
geneview	rs527236060
scholar	rs527236060
google	rs527236060
pharmgkb	rs527236060
gwascentral	rs527236060
openSNP	rs527236060
23andMe	rs527236060
SNPshot	rs527236060
SNPdbe	rs527236060
MSV3d	rs527236060
GWAS Ctlg	rs527236060

Max Magnitude

0

ClinVar
Risk	rs527236060(A;A) rs527236060(C;C)
Alt	rs527236060(A;A) rs527236060(C;C)
Reference	Rs527236060(G;G)
Significance	Probable-Pathogenic
Disease	Retinitis pigmentosa
Variation	info
Gene	CNGB1
CLNDBN	Retinitis pigmentosa
Reversed	1
HGVS	NC_000016.9:g.57998386C>G
CLNSRC	ClinVar
CLNACC	RCV000132646.1,