rs62638625

Orientation

minus

Stabilized

minus

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

Make rs62638625(A;A)

Make rs62638625(A;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

178983005

Gene

GRM6

is a	snp
is	mentioned by
dbSNP	rs62638625
dbSNP (classic)	rs62638625
ClinGen	rs62638625
ebi	rs62638625
HLI	rs62638625
Exac	rs62638625
Gnomad	rs62638625
Varsome	rs62638625
LitVar	rs62638625
Map	rs62638625
PheGenI	rs62638625
Biobank	rs62638625
1000 genomes	rs62638625
hgdp	rs62638625
ensembl	rs62638625
geneview	rs62638625
scholar	rs62638625
google	rs62638625
pharmgkb	rs62638625
gwascentral	rs62638625
openSNP	rs62638625
23andMe	rs62638625
SNPshot	rs62638625
SNPdbe	rs62638625
MSV3d	rs62638625
GWAS Ctlg	rs62638625

Max Magnitude

0

OMIM	604096
Desc
Variant	0002
Related	also

ClinVar
Risk	rs62638625(A;A)
Alt	rs62638625(A;A)
Reference	Rs62638625(G;G)
Significance	Pathogenic
Disease	Congenital stationary night blindness not provided
Variation	info
Gene	GRM6
CLNDBN	Congenital stationary night blindness, type 1B not provided
Reversed	1
HGVS	NC_000005.9:g.178410006C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006198.3, RCV000086047.1,