rs878853383

Orientation

plus

Stabilized

plus

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

Make rs878853383(-;-)

Make rs878853383(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

47839672

Gene

CRX

is a	snp
is	mentioned by
dbSNP	rs878853383
dbSNP (classic)	rs878853383
ClinGen	rs878853383
ebi	rs878853383
HLI	rs878853383
Exac	rs878853383
Gnomad	rs878853383
Varsome	rs878853383
LitVar	rs878853383
Map	rs878853383
PheGenI	rs878853383
Biobank	rs878853383
1000 genomes	rs878853383
hgdp	rs878853383
ensembl	rs878853383
geneview	rs878853383
scholar	rs878853383
google	rs878853383
pharmgkb	rs878853383
gwascentral	rs878853383
openSNP	rs878853383
23andMe	rs878853383
SNPshot	rs878853383
SNPdbe	rs878853383
MSV3d	rs878853383
GWAS Ctlg	rs878853383

Max Magnitude

0

ClinVar
Risk	rs878853383(-;-)
Alt	rs878853383(-;-)
Reference	Rs878853383(G;G)
Significance	Probable-Pathogenic
Disease	Retinal dystrophy
Variation	info
Gene	CRX
CLNDBN	Retinal dystrophy
Reversed	0
HGVS	NC_000019.9:g.48342929delG
CLNSRC
CLNACC	RCV000225573.1,