rs878853366

Orientation

plus

Stabilized

plus

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

Make rs878853366(-;A)

Make rs878853366(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

197344435

Gene

CRB1

is a	snp
is	mentioned by
dbSNP	rs878853366
dbSNP (classic)	rs878853366
ClinGen	rs878853366
ebi	rs878853366
HLI	rs878853366
Exac	rs878853366
Gnomad	rs878853366
Varsome	rs878853366
LitVar	rs878853366
Map	rs878853366
PheGenI	rs878853366
Biobank	rs878853366
1000 genomes	rs878853366
hgdp	rs878853366
ensembl	rs878853366
geneview	rs878853366
scholar	rs878853366
google	rs878853366
pharmgkb	rs878853366
gwascentral	rs878853366
openSNP	rs878853366
23andMe	rs878853366
SNPshot	rs878853366
SNPdbe	rs878853366
MSV3d	rs878853366
GWAS Ctlg	rs878853366

Max Magnitude

0

ClinVar
Risk	rs878853366(A;A)
Alt	rs878853366(A;A)
Reference	Rs878853366(-;-)
Significance	Probable-Pathogenic
Disease	Retinal dystrophy
Variation	info
Gene	CRB1
CLNDBN	Retinal dystrophy
Reversed	0
HGVS	NC_000001.10:g.197313565dupA
CLNSRC
CLNACC	RCV000225488.1,