rs62638197

Orientation

minus

Stabilized

minus

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

Make rs62638197(C;T)

Make rs62638197(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

178994808

Gene

GRM6

is a	snp
is	mentioned by
dbSNP	rs62638197
dbSNP (classic)	rs62638197
ClinGen	rs62638197
ebi	rs62638197
HLI	rs62638197
Exac	rs62638197
Gnomad	rs62638197
Varsome	rs62638197
LitVar	rs62638197
Map	rs62638197
PheGenI	rs62638197
Biobank	rs62638197
1000 genomes	rs62638197
hgdp	rs62638197
ensembl	rs62638197
geneview	rs62638197
scholar	rs62638197
google	rs62638197
pharmgkb	rs62638197
gwascentral	rs62638197
openSNP	rs62638197
23andMe	rs62638197
SNPshot	rs62638197
SNPdbe	rs62638197
MSV3d	rs62638197
GWAS Ctlg	rs62638197

Max Magnitude

0

OMIM	604096
Desc
Variant	0005
Related	also

ClinVar
Risk	rs62638197(T;T)
Alt	rs62638197(T;T)
Reference	Rs62638197(C;C)
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.178421809G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006201.4, RCV000086025.1,