rs121434621

Orientation

plus

Stabilized

plus

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

Make rs121434621(C;C)

Make rs121434621(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154154602

Gene

OPN1LW

is a	snp
is	mentioned by
dbSNP	rs121434621
dbSNP (classic)	rs121434621
ClinGen	rs121434621
ebi	rs121434621
HLI	rs121434621
Exac	rs121434621
Gnomad	rs121434621
Varsome	rs121434621
LitVar	rs121434621
Map	rs121434621
PheGenI	rs121434621
Biobank	rs121434621
1000 genomes	rs121434621
hgdp	rs121434621
ensembl	rs121434621
geneview	rs121434621
scholar	rs121434621
google	rs121434621
pharmgkb	rs121434621
gwascentral	rs121434621
openSNP	rs121434621
23andMe	rs121434621
SNPshot	rs121434621
SNPdbe	rs121434621
MSV3d	rs121434621
GWAS Ctlg	rs121434621

Max Magnitude

0

ClinVar
Risk	rs121434621(C;C)
Alt	rs121434621(C;C)
Reference	Rs121434621(T;T)
Significance	Pathogenic
Disease	Cone monochromatism not provided
Variation	info
Gene	OPN1LW
CLNDBN	Cone monochromatism not provided
Reversed	0
HGVS	NC_000023.10:g.153420077T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011251.6, RCV000479007.1,