rs104894912

Orientation

plus

Stabilized

plus

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

Make rs104894912(C;T)

Make rs104894912(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154154734

Gene

OPN1LW

is a	snp
is	mentioned by
dbSNP	rs104894912
dbSNP (classic)	rs104894912
ClinGen	rs104894912
ebi	rs104894912
HLI	rs104894912
Exac	rs104894912
Gnomad	rs104894912
Varsome	rs104894912
LitVar	rs104894912
Map	rs104894912
PheGenI	rs104894912
Biobank	rs104894912
1000 genomes	rs104894912
hgdp	rs104894912
ensembl	rs104894912
geneview	rs104894912
scholar	rs104894912
google	rs104894912
pharmgkb	rs104894912
gwascentral	rs104894912
openSNP	rs104894912
23andMe	rs104894912
SNPshot	rs104894912
SNPdbe	rs104894912
MSV3d	rs104894912
GWAS Ctlg	rs104894912

Max Magnitude

0

ClinVar
Risk	rs104894912(T;T)
Alt	rs104894912(T;T)
Reference	Rs104894912(C;C)
Significance	Pathogenic
Disease	Cone monochromatism
Variation	info
Gene	OPN1LW
CLNDBN	Cone monochromatism
Reversed	0
HGVS	NC_000023.10:g.153420209C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011249.7,