rs267606927

Orientation

plus

Stabilized

plus

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

Make rs267606927(C;C)

Make rs267606927(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154190173

Gene

OPN1MW

is a	snp
is	mentioned by
dbSNP	rs267606927
dbSNP (classic)	rs267606927
ClinGen	rs267606927
ebi	rs267606927
HLI	rs267606927
Exac	rs267606927
Gnomad	rs267606927
Varsome	rs267606927
LitVar	rs267606927
Map	rs267606927
PheGenI	rs267606927
Biobank	rs267606927
1000 genomes	rs267606927
hgdp	rs267606927
ensembl	rs267606927
geneview	rs267606927
scholar	rs267606927
google	rs267606927
pharmgkb	rs267606927
gwascentral	rs267606927
openSNP	rs267606927
23andMe	rs267606927
SNPshot	rs267606927
SNPdbe	rs267606927
MSV3d	rs267606927
GWAS Ctlg	rs267606927

Max Magnitude

0

ClinVar
Risk	rs267606927(C;C)
Alt	rs267606927(C;C)
Reference	Rs267606927(T;T)
Significance	Pathogenic
Disease	Cone dystrophy 5
Variation	info
Gene	OPN1MW
CLNDBN	Cone dystrophy 5, X-linked
Reversed	0
HGVS	NC_000023.10:g.153455662T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000011259.7,