rs1057517886

Orientation

minus

Stabilized

minus

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

Make rs1057517886(A;T)

Make rs1057517886(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

88139174

Gene

CEP290

is a	snp
is	mentioned by
dbSNP	rs1057517886
dbSNP (classic)	rs1057517886
ClinGen	rs1057517886
ebi	rs1057517886
HLI	rs1057517886
Exac	rs1057517886
Gnomad	rs1057517886
Varsome	rs1057517886
LitVar	rs1057517886
Map	rs1057517886
PheGenI	rs1057517886
Biobank	rs1057517886
1000 genomes	rs1057517886
hgdp	rs1057517886
ensembl	rs1057517886
geneview	rs1057517886
scholar	rs1057517886
google	rs1057517886
pharmgkb	rs1057517886
gwascentral	rs1057517886
openSNP	rs1057517886
23andMe	rs1057517886
SNPshot	rs1057517886
SNPdbe	rs1057517886
MSV3d	rs1057517886
GWAS Ctlg	rs1057517886

Max Magnitude

0

ClinVar
Risk	rs1057517886(T;T)
Alt	rs1057517886(T;T)
Reference	Rs1057517886(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CEP290
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.88532951T>A
CLNSRC
CLNACC	RCV000413097.1,