rs766470795

Orientation

plus

Stabilized

plus

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

Make rs766470795(A;A)

Make rs766470795(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

123373794

Gene

CRB2

is a	snp
is	mentioned by
dbSNP	rs766470795
dbSNP (classic)	rs766470795
ClinGen	rs766470795
ebi	rs766470795
HLI	rs766470795
Exac	rs766470795
Gnomad	rs766470795
Varsome	rs766470795
LitVar	rs766470795
Map	rs766470795
PheGenI	rs766470795
Biobank	rs766470795
1000 genomes	rs766470795
hgdp	rs766470795
ensembl	rs766470795
geneview	rs766470795
scholar	rs766470795
google	rs766470795
pharmgkb	rs766470795
gwascentral	rs766470795
openSNP	rs766470795
23andMe	rs766470795
SNPshot	rs766470795
SNPdbe	rs766470795
MSV3d	rs766470795
GWAS Ctlg	rs766470795

Max Magnitude

0

ClinVar
Risk	rs766470795(A;A)
Alt	rs766470795(A;A)
Reference	Rs766470795(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CRB2
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.126136073G>A
CLNSRC
CLNACC	RCV000494573.1,