rs104894916

Orientation

plus

Stabilized

plus

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

Make rs104894916(A;A)

Make rs104894916(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154195934

Gene

OPN1MW

is a	snp
is	mentioned by
dbSNP	rs104894916
dbSNP (classic)	rs104894916
ClinGen	rs104894916
ebi	rs104894916
HLI	rs104894916
Exac	rs104894916
Gnomad	rs104894916
Varsome	rs104894916
LitVar	rs104894916
Map	rs104894916
PheGenI	rs104894916
Biobank	rs104894916
1000 genomes	rs104894916
hgdp	rs104894916
ensembl	rs104894916
geneview	rs104894916
scholar	rs104894916
google	rs104894916
pharmgkb	rs104894916
gwascentral	rs104894916
openSNP	rs104894916
23andMe	rs104894916
SNPshot	rs104894916
SNPdbe	rs104894916
MSV3d	rs104894916
GWAS Ctlg	rs104894916

Merged from

Rs28935199

Max Magnitude

0

OMIM	300821
Desc
Variant	0004
Related	also

ClinVar
Risk	rs104894916(A;A)
Alt	rs104894916(A;A)
Reference	Rs104894916(G;G)
Significance	Pathogenic
Disease	Colorblindness
Variation	info
Gene	OPN1MW
CLNDBN	Colorblindness, partial, deutan series
Reversed	0
HGVS	NC_000023.10:g.153461425G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000011255.5,