rs1057517052

Orientation

minus

Stabilized

minus

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

Make rs1057517052(-;-)

Make rs1057517052(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

86668095

Gene

CNGB3

is a	snp
is	mentioned by
dbSNP	rs1057517052
dbSNP (classic)	rs1057517052
ClinGen	rs1057517052
ebi	rs1057517052
HLI	rs1057517052
Exac	rs1057517052
Gnomad	rs1057517052
Varsome	rs1057517052
LitVar	rs1057517052
Map	rs1057517052
PheGenI	rs1057517052
Biobank	rs1057517052
1000 genomes	rs1057517052
hgdp	rs1057517052
ensembl	rs1057517052
geneview	rs1057517052
scholar	rs1057517052
google	rs1057517052
pharmgkb	rs1057517052
gwascentral	rs1057517052
openSNP	rs1057517052
23andMe	rs1057517052
SNPshot	rs1057517052
SNPdbe	rs1057517052
MSV3d	rs1057517052
GWAS Ctlg	rs1057517052

Max Magnitude

0

ClinVar
Risk	rs1057517052(-;-)
Alt	rs1057517052(-;-)
Reference	Rs1057517052(G;G)
Significance	Probable-Pathogenic
Disease	Achromatopsia 3
Variation	info
Gene	CNGB3
CLNDBN	Achromatopsia 3
Reversed	1
HGVS	NC_000008.10:g.87680323delC
CLNSRC
CLNACC	RCV000411187.1,