rs1057516866

Orientation

minus

Stabilized

minus

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

Make rs1057516866(-;-)

Make rs1057516866(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

86632812

Gene

CNGB3

is a	snp
is	mentioned by
dbSNP	rs1057516866
dbSNP (classic)	rs1057516866
ClinGen	rs1057516866
ebi	rs1057516866
HLI	rs1057516866
Exac	rs1057516866
Gnomad	rs1057516866
Varsome	rs1057516866
LitVar	rs1057516866
Map	rs1057516866
PheGenI	rs1057516866
Biobank	rs1057516866
1000 genomes	rs1057516866
hgdp	rs1057516866
ensembl	rs1057516866
geneview	rs1057516866
scholar	rs1057516866
google	rs1057516866
pharmgkb	rs1057516866
gwascentral	rs1057516866
openSNP	rs1057516866
23andMe	rs1057516866
SNPshot	rs1057516866
SNPdbe	rs1057516866
MSV3d	rs1057516866
GWAS Ctlg	rs1057516866

Max Magnitude

0

ClinVar
Risk	rs1057516866(-;-)
Alt	rs1057516866(-;-)
Reference	Rs1057516866(T;T)
Significance	Probable-Pathogenic
Disease	Achromatopsia 3
Variation	info
Gene	CNGB3
CLNDBN	Achromatopsia 3
Reversed	1
HGVS	NC_000008.10:g.87645040delA
CLNSRC
CLNACC	RCV000411676.1,