rs1064794342

Orientation

minus

Stabilized

minus

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

Chromosome

16

Position

57903851

Gene

CNGB1

is a	snp
is	mentioned by
dbSNP	rs1064794342
dbSNP (classic)	rs1064794342
ClinGen	rs1064794342
ebi	rs1064794342
HLI	rs1064794342
Exac	rs1064794342
Gnomad	rs1064794342
Varsome	rs1064794342
LitVar	rs1064794342
Map	rs1064794342
PheGenI	rs1064794342
Biobank	rs1064794342
1000 genomes	rs1064794342
hgdp	rs1064794342
ensembl	rs1064794342
geneview	rs1064794342
scholar	rs1064794342
google	rs1064794342
pharmgkb	rs1064794342
gwascentral	rs1064794342
openSNP	rs1064794342
23andMe	rs1064794342
SNPshot	rs1064794342
SNPdbe	rs1064794342
MSV3d	rs1064794342
GWAS Ctlg	rs1064794342

Max Magnitude

0

ClinVar
Risk	rs1064794342(-;-)
Alt	rs1064794342(-;-)
Reference	Rs1064794342(ACGA;ACGA)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CNGB1
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.57937755_57937758delTCGT
CLNSRC
CLNACC	RCV000479018.1,