rs878853364

Orientation

plus

Stabilized

plus

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

Make rs878853364(-;CTTA)

Make rs878853364(CTTA;CTTA)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

197421440

Gene

CRB1

is a	snp
is	mentioned by
dbSNP	rs878853364
dbSNP (classic)	rs878853364
ClinGen	rs878853364
ebi	rs878853364
HLI	rs878853364
Exac	rs878853364
Gnomad	rs878853364
Varsome	rs878853364
LitVar	rs878853364
Map	rs878853364
PheGenI	rs878853364
Biobank	rs878853364
1000 genomes	rs878853364
hgdp	rs878853364
ensembl	rs878853364
geneview	rs878853364
scholar	rs878853364
google	rs878853364
pharmgkb	rs878853364
gwascentral	rs878853364
openSNP	rs878853364
23andMe	rs878853364
SNPshot	rs878853364
SNPdbe	rs878853364
MSV3d	rs878853364
GWAS Ctlg	rs878853364

Max Magnitude

0

ClinVar
Risk	rs878853364(CTTA;CTTA)
Alt	rs878853364(CTTA;CTTA)
Reference	Rs878853364(-;-)
Significance	Probable-Pathogenic
Disease	Retinal dystrophy
Variation	info
Gene	CRB1
CLNDBN	Retinal dystrophy
Reversed	0
HGVS	NC_000001.10:g.197390570_197390571insCTTA
CLNSRC
CLNACC	RCV000225570.1,