rs786204762

Orientation

minus

Stabilized

minus

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

Make rs786204762(A;A)

Make rs786204762(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

86643810

Gene

CNGB3

is a	snp
is	mentioned by
dbSNP	rs786204762
dbSNP (classic)	rs786204762
ClinGen	rs786204762
ebi	rs786204762
HLI	rs786204762
Exac	rs786204762
Gnomad	rs786204762
Varsome	rs786204762
LitVar	rs786204762
Map	rs786204762
PheGenI	rs786204762
Biobank	rs786204762
1000 genomes	rs786204762
hgdp	rs786204762
ensembl	rs786204762
geneview	rs786204762
scholar	rs786204762
google	rs786204762
pharmgkb	rs786204762
gwascentral	rs786204762
openSNP	rs786204762
23andMe	rs786204762
SNPshot	rs786204762
SNPdbe	rs786204762
MSV3d	rs786204762
GWAS Ctlg	rs786204762

Max Magnitude

0

ClinVar
Risk	rs786204762(A;A)
Alt	rs786204762(A;A)
Reference	Rs786204762(G;G)
Significance	Pathogenic
Disease	Achromatopsia 3 not provided
Variation	info
Gene	CNGB3
CLNDBN	Achromatopsia 3 not provided
Reversed	1
HGVS	NC_000008.10:g.87656038C>T
CLNSRC
CLNACC	RCV000169624.1, RCV000255345.1,