rs1057516878

Orientation

minus

Stabilized

minus

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

Make rs1057516878(-;-)

Make rs1057516878(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

86629033

Gene

CNGB3

is a	snp
is	mentioned by
dbSNP	rs1057516878
dbSNP (classic)	rs1057516878
ClinGen	rs1057516878
ebi	rs1057516878
HLI	rs1057516878
Exac	rs1057516878
Gnomad	rs1057516878
Varsome	rs1057516878
LitVar	rs1057516878
Map	rs1057516878
PheGenI	rs1057516878
Biobank	rs1057516878
1000 genomes	rs1057516878
hgdp	rs1057516878
ensembl	rs1057516878
geneview	rs1057516878
scholar	rs1057516878
google	rs1057516878
pharmgkb	rs1057516878
gwascentral	rs1057516878
openSNP	rs1057516878
23andMe	rs1057516878
SNPshot	rs1057516878
SNPdbe	rs1057516878
MSV3d	rs1057516878
GWAS Ctlg	rs1057516878

Max Magnitude

0

ClinVar
Risk	rs1057516878(-;-)
Alt	rs1057516878(-;-)
Reference	Rs1057516878(C;C)
Significance	Probable-Pathogenic
Disease	Achromatopsia 3
Variation	info
Gene	CNGB3
CLNDBN	Achromatopsia 3
Reversed	1
HGVS	NC_000008.10:g.87641261delG
CLNSRC
CLNACC	RCV000410652.1,