rs786204492

Orientation

minus

Stabilized

minus

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

Make rs786204492(C;T)

Make rs786204492(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

86671046

Gene

CNGB3

is a	snp
is	mentioned by
dbSNP	rs786204492
dbSNP (classic)	rs786204492
ClinGen	rs786204492
ebi	rs786204492
HLI	rs786204492
Exac	rs786204492
Gnomad	rs786204492
Varsome	rs786204492
LitVar	rs786204492
Map	rs786204492
PheGenI	rs786204492
Biobank	rs786204492
1000 genomes	rs786204492
hgdp	rs786204492
ensembl	rs786204492
geneview	rs786204492
scholar	rs786204492
google	rs786204492
pharmgkb	rs786204492
gwascentral	rs786204492
openSNP	rs786204492
23andMe	rs786204492
SNPshot	rs786204492
SNPdbe	rs786204492
MSV3d	rs786204492
GWAS Ctlg	rs786204492

Max Magnitude

0

ClinVar
Risk	rs786204492(T;T)
Alt	rs786204492(T;T)
Reference	Rs786204492(C;C)
Significance	Probable-Pathogenic
Disease	Achromatopsia 3
Variation	info
Gene	CNGB3
CLNDBN	Achromatopsia 3
Reversed	1
HGVS	NC_000008.10:g.87683274G>A
CLNSRC
CLNACC	RCV000169161.1,