rs62638202

Orientation

minus

Stabilized

minus

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

Make rs62638202(A;A)

Make rs62638202(A;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

178994497

Gene

GRM6

is a	snp
is	mentioned by
dbSNP	rs62638202
dbSNP (classic)	rs62638202
ClinGen	rs62638202
ebi	rs62638202
HLI	rs62638202
Exac	rs62638202
Gnomad	rs62638202
Varsome	rs62638202
LitVar	rs62638202
Map	rs62638202
PheGenI	rs62638202
Biobank	rs62638202
1000 genomes	rs62638202
hgdp	rs62638202
ensembl	rs62638202
geneview	rs62638202
scholar	rs62638202
google	rs62638202
pharmgkb	rs62638202
gwascentral	rs62638202
openSNP	rs62638202
23andMe	rs62638202
SNPshot	rs62638202
SNPdbe	rs62638202
MSV3d	rs62638202
GWAS Ctlg	rs62638202

Max Magnitude

0

OMIM	604096
Desc
Variant	0004
Related	also

ClinVar
Risk	rs62638202(A;A)
Alt	rs62638202(A;A)
Reference	Rs62638202(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.178421498C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006200.3, RCV000086056.1,