rs387907138

Orientation

minus

Stabilized

minus

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

Make rs387907138(C;T)

Make rs387907138(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

38343192

Gene

GPR179

is a	snp
is	mentioned by
dbSNP	rs387907138
dbSNP (classic)	rs387907138
ClinGen	rs387907138
ebi	rs387907138
HLI	rs387907138
Exac	rs387907138
Gnomad	rs387907138
Varsome	rs387907138
LitVar	rs387907138
Map	rs387907138
PheGenI	rs387907138
Biobank	rs387907138
1000 genomes	rs387907138
hgdp	rs387907138
ensembl	rs387907138
geneview	rs387907138
scholar	rs387907138
google	rs387907138
pharmgkb	rs387907138
gwascentral	rs387907138
openSNP	rs387907138
23andMe	rs387907138
SNPshot	rs387907138
SNPdbe	rs387907138
MSV3d	rs387907138
GWAS Ctlg	rs387907138

Max Magnitude

0

ClinVar
Risk	rs387907138(T;T)
Alt	rs387907138(T;T)
Reference	Rs387907138(C;C)
Significance	Pathogenic
Disease	Congenital stationary night blindness
Variation	info
Gene	GPR179
CLNDBN	Congenital stationary night blindness, type 1E
Reversed	1
HGVS	NC_000017.10:g.36499075G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000024201.3,