rs527236061

Orientation

minus

Stabilized

minus

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

Make rs527236061(-;A)

Make rs527236061(A;A)

Reference

GRCh38 38.1/142

Chromosome

16

Position

57904843

Gene

CNGB1

is a	snp
is	mentioned by
dbSNP	rs527236061
dbSNP (classic)	rs527236061
ClinGen	rs527236061
ebi	rs527236061
HLI	rs527236061
Exac	rs527236061
Gnomad	rs527236061
Varsome	rs527236061
LitVar	rs527236061
Map	rs527236061
PheGenI	rs527236061
Biobank	rs527236061
1000 genomes	rs527236061
hgdp	rs527236061
ensembl	rs527236061
geneview	rs527236061
scholar	rs527236061
google	rs527236061
pharmgkb	rs527236061
gwascentral	rs527236061
openSNP	rs527236061
23andMe	rs527236061
SNPshot	rs527236061
SNPdbe	rs527236061
MSV3d	rs527236061
GWAS Ctlg	rs527236061

Max Magnitude

0

ClinVar
Risk	rs527236061(A;A)
Alt	rs527236061(A;A)
Reference	Rs527236061(-;-)
Significance	Probable-Pathogenic
Disease	Retinitis pigmentosa
Variation	info
Gene	CNGB1
CLNDBN	Retinitis pigmentosa
Reversed	1
HGVS	NC_000016.9:g.57938748dupT
CLNSRC	ClinVar
CLNACC	RCV000132647.1,