rs104894913

Orientation

plus

Stabilized

plus

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

Make rs104894913(A;A)

Make rs104894913(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154158844

Gene

OPN1LW

is a	snp
is	mentioned by
dbSNP	rs104894913
dbSNP (classic)	rs104894913
ClinGen	rs104894913
ebi	rs104894913
HLI	rs104894913
Exac	rs104894913
Gnomad	rs104894913
Varsome	rs104894913
LitVar	rs104894913
Map	rs104894913
PheGenI	rs104894913
Biobank	rs104894913
1000 genomes	rs104894913
hgdp	rs104894913
ensembl	rs104894913
geneview	rs104894913
scholar	rs104894913
google	rs104894913
pharmgkb	rs104894913
gwascentral	rs104894913
openSNP	rs104894913
23andMe	rs104894913
SNPshot	rs104894913
SNPdbe	rs104894913
MSV3d	rs104894913
GWAS Ctlg	rs104894913

Max Magnitude

0

ClinVar
Risk	rs104894913(A;A)
Alt	rs104894913(A;A)
Reference	Rs104894913(G;G)
Significance	Pathogenic
Disease	Protan defect
Variation	info
Gene	OPN1LW
CLNDBN	Protan defect
Reversed	0
HGVS	NC_000023.10:g.153424319G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011252.3,