rs1057517167

Orientation

minus

Stabilized

minus

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

Make rs1057517167(A;T)

Make rs1057517167(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

86632895

Gene

CNGB3

is a	snp
is	mentioned by
dbSNP	rs1057517167
dbSNP (classic)	rs1057517167
ClinGen	rs1057517167
ebi	rs1057517167
HLI	rs1057517167
Exac	rs1057517167
Gnomad	rs1057517167
Varsome	rs1057517167
LitVar	rs1057517167
Map	rs1057517167
PheGenI	rs1057517167
Biobank	rs1057517167
1000 genomes	rs1057517167
hgdp	rs1057517167
ensembl	rs1057517167
geneview	rs1057517167
scholar	rs1057517167
google	rs1057517167
pharmgkb	rs1057517167
gwascentral	rs1057517167
openSNP	rs1057517167
23andMe	rs1057517167
SNPshot	rs1057517167
SNPdbe	rs1057517167
MSV3d	rs1057517167
GWAS Ctlg	rs1057517167

Max Magnitude

0

ClinVar
Risk	rs1057517167(T;T)
Alt	rs1057517167(T;T)
Reference	Rs1057517167(A;A)
Significance	Probable-Pathogenic
Disease	Achromatopsia 3
Variation	info
Gene	CNGB3
CLNDBN	Achromatopsia 3
Reversed	1
HGVS	NC_000008.10:g.87645123T>A
CLNSRC
CLNACC	RCV000412299.1,