rs62638624

Orientation

minus

Stabilized

minus

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

Make rs62638624(C;T)

Make rs62638624(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

178986132

Gene

GRM6

is a	snp
is	mentioned by
dbSNP	rs62638624
dbSNP (classic)	rs62638624
ClinGen	rs62638624
ebi	rs62638624
HLI	rs62638624
Exac	rs62638624
Gnomad	rs62638624
Varsome	rs62638624
LitVar	rs62638624
Map	rs62638624
PheGenI	rs62638624
Biobank	rs62638624
1000 genomes	rs62638624
hgdp	rs62638624
ensembl	rs62638624
geneview	rs62638624
scholar	rs62638624
google	rs62638624
pharmgkb	rs62638624
gwascentral	rs62638624
openSNP	rs62638624
23andMe	rs62638624
SNPshot	rs62638624
SNPdbe	rs62638624
MSV3d	rs62638624
GWAS Ctlg	rs62638624

Max Magnitude

0

OMIM	604096
Desc
Variant	0003
Related	also

ClinVar
Risk	rs62638624(T;T)
Alt	rs62638624(T;T)
Reference	Rs62638624(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.178413133G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006199.3, RCV000086044.1,