rs768345097

Orientation

plus

Stabilized

plus

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

Make rs768345097(A;A)

Make rs768345097(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

86667131

Gene

CNGB3

is a	snp
is	mentioned by
dbSNP	rs768345097
dbSNP (classic)	rs768345097
ClinGen	rs768345097
ebi	rs768345097
HLI	rs768345097
Exac	rs768345097
Gnomad	rs768345097
Varsome	rs768345097
LitVar	rs768345097
Map	rs768345097
PheGenI	rs768345097
Biobank	rs768345097
1000 genomes	rs768345097
hgdp	rs768345097
ensembl	rs768345097
geneview	rs768345097
scholar	rs768345097
google	rs768345097
pharmgkb	rs768345097
gwascentral	rs768345097
openSNP	rs768345097
23andMe	rs768345097
SNPshot	rs768345097
SNPdbe	rs768345097
MSV3d	rs768345097
GWAS Ctlg	rs768345097

Max Magnitude

0

ClinVar
Risk	rs768345097(A;A)
Alt	rs768345097(A;A)
Reference	Rs768345097(G;G)
Significance	Probable-Pathogenic
Disease	Achromatopsia 3
Variation	info
Gene	CNGB3
CLNDBN	Achromatopsia 3
Reversed	0
HGVS	NC_000008.10:g.87679359G>A
CLNSRC
CLNACC	RCV000169194.1,