rs770066665

Orientation

plus

Stabilized

plus

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

Make rs770066665(-;-)

Make rs770066665(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

38337640

Gene

GPR179

is a	snp
is	mentioned by
dbSNP	rs770066665
dbSNP (classic)	rs770066665
ClinGen	rs770066665
ebi	rs770066665
HLI	rs770066665
Exac	rs770066665
Gnomad	rs770066665
Varsome	rs770066665
LitVar	rs770066665
Map	rs770066665
PheGenI	rs770066665
Biobank	rs770066665
1000 genomes	rs770066665
hgdp	rs770066665
ensembl	rs770066665
geneview	rs770066665
scholar	rs770066665
google	rs770066665
pharmgkb	rs770066665
gwascentral	rs770066665
openSNP	rs770066665
23andMe	rs770066665
SNPshot	rs770066665
SNPdbe	rs770066665
MSV3d	rs770066665
GWAS Ctlg	rs770066665

Max Magnitude

0

ClinVar
Risk	rs770066665(-;-)
Alt	rs770066665(-;-)
Reference	Rs770066665(G;G)
Significance	Pathogenic
Disease	Congenital stationary night blindness not provided Congenital Stationary Night Blindness
Variation	info
Gene	GPR179
CLNDBN	Congenital stationary night blindness, type 1E not provided Congenital Stationary Night Blindness, Recessive
Reversed	0
HGVS	NC_000017.10:g.36493523delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000024203.3, RCV000309713.1, RCV000318580.1,