rs724159983

Orientation

plus

Stabilized

plus

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

Make rs724159983(A;C)

Make rs724159983(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

154182566

Gene

OPN1MW

is a	snp
is	mentioned by
dbSNP	rs724159983
dbSNP (classic)	rs724159983
ClinGen	rs724159983
ebi	rs724159983
HLI	rs724159983
Exac	rs724159983
Gnomad	rs724159983
Varsome	rs724159983
LitVar	rs724159983
Map	rs724159983
PheGenI	rs724159983
Biobank	rs724159983
1000 genomes	rs724159983
hgdp	rs724159983
ensembl	rs724159983
geneview	rs724159983
scholar	rs724159983
google	rs724159983
pharmgkb	rs724159983
gwascentral	rs724159983
openSNP	rs724159983
23andMe	rs724159983
SNPshot	rs724159983
SNPdbe	rs724159983
MSV3d	rs724159983
GWAS Ctlg	rs724159983

Max Magnitude

0

ClinVar
Risk	rs724159983(C;C)
Alt	rs724159983(C;C)
Reference	Rs724159983(A;A)
Significance	Pathogenic
Disease	Colorblindness
Variation	info
Gene	OPN1MW
CLNDBN	Colorblindness, partial, deutan series
Reversed	0
HGVS	NC_000023.10:g.153448055A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011256.3,