rs1057516825

Orientation

minus

Stabilized

minus

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

Make rs1057516825(A;A)

Make rs1057516825(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

86628918

Gene

CNGB3

is a	snp
is	mentioned by
dbSNP	rs1057516825
dbSNP (classic)	rs1057516825
ClinGen	rs1057516825
ebi	rs1057516825
HLI	rs1057516825
Exac	rs1057516825
Gnomad	rs1057516825
Varsome	rs1057516825
LitVar	rs1057516825
Map	rs1057516825
PheGenI	rs1057516825
Biobank	rs1057516825
1000 genomes	rs1057516825
hgdp	rs1057516825
ensembl	rs1057516825
geneview	rs1057516825
scholar	rs1057516825
google	rs1057516825
pharmgkb	rs1057516825
gwascentral	rs1057516825
openSNP	rs1057516825
23andMe	rs1057516825
SNPshot	rs1057516825
SNPdbe	rs1057516825
MSV3d	rs1057516825
GWAS Ctlg	rs1057516825

Max Magnitude

0

ClinVar
Risk	rs1057516825(A;A)
Alt	rs1057516825(A;A)
Reference	Rs1057516825(G;G)
Significance	Probable-Pathogenic
Disease	Achromatopsia 3
Variation	info
Gene	CNGB3
CLNDBN	Achromatopsia 3
Reversed	1
HGVS	NC_000008.10:g.87641146C>T
CLNSRC
CLNACC	RCV000412081.1,