rs62638208

Orientation

minus

Stabilized

minus

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

Make rs62638208(A;A)

Make rs62638208(A;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

178986689

Gene

GRM6

is a	snp
is	mentioned by
dbSNP	rs62638208
dbSNP (classic)	rs62638208
ClinGen	rs62638208
ebi	rs62638208
HLI	rs62638208
Exac	rs62638208
Gnomad	rs62638208
Varsome	rs62638208
LitVar	rs62638208
Map	rs62638208
PheGenI	rs62638208
Biobank	rs62638208
1000 genomes	rs62638208
hgdp	rs62638208
ensembl	rs62638208
geneview	rs62638208
scholar	rs62638208
google	rs62638208
pharmgkb	rs62638208
gwascentral	rs62638208
openSNP	rs62638208
23andMe	rs62638208
SNPshot	rs62638208
SNPdbe	rs62638208
MSV3d	rs62638208
GWAS Ctlg	rs62638208

Max Magnitude

0

OMIM	604096
Desc
Variant	0007
Related	also

ClinVar
Risk	rs62638208(A;A)
Alt	rs62638208(A;A)
Reference	Rs62638208(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.178413690C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006203.3, RCV000086028.1,