rs121434304

Orientation

minus

Stabilized

minus

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

Make rs121434304(C;C)

Make rs121434304(C;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

178989075

Gene

GRM6

is a	snp
is	mentioned by
dbSNP	rs121434304
dbSNP (classic)	rs121434304
ClinGen	rs121434304
ebi	rs121434304
HLI	rs121434304
Exac	rs121434304
Gnomad	rs121434304
Varsome	rs121434304
LitVar	rs121434304
Map	rs121434304
PheGenI	rs121434304
Biobank	rs121434304
1000 genomes	rs121434304
hgdp	rs121434304
ensembl	rs121434304
geneview	rs121434304
scholar	rs121434304
google	rs121434304
pharmgkb	rs121434304
gwascentral	rs121434304
openSNP	rs121434304
23andMe	rs121434304
SNPshot	rs121434304
SNPdbe	rs121434304
MSV3d	rs121434304
GWAS Ctlg	rs121434304

Max Magnitude

0

OMIM	604096
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121434304(C;C)
Alt	rs121434304(C;C)
Reference	Rs121434304(T;T)
Significance	Other
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.178416076A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006204.4, RCV000439410.1,