rs62637021

Orientation

plus

Stabilized

plus

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

Make rs62637021(A;A)

Make rs62637021(A;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

41473558

Gene

NYX

is a	snp
is	mentioned by
dbSNP	rs62637021
dbSNP (classic)	rs62637021
ClinGen	rs62637021
ebi	rs62637021
HLI	rs62637021
Exac	rs62637021
Gnomad	rs62637021
Varsome	rs62637021
LitVar	rs62637021
Map	rs62637021
PheGenI	rs62637021
Biobank	rs62637021
1000 genomes	rs62637021
hgdp	rs62637021
ensembl	rs62637021
geneview	rs62637021
scholar	rs62637021
google	rs62637021
pharmgkb	rs62637021
gwascentral	rs62637021
openSNP	rs62637021
23andMe	rs62637021
SNPshot	rs62637021
SNPdbe	rs62637021
MSV3d	rs62637021
GWAS Ctlg	rs62637021

Max Magnitude

0

OMIM	300278
Desc
Variant	0003
Related	also

ClinVar
Risk	rs62637021(A;A)
Alt	rs62637021(A;A)
Reference	Rs62637021(C;C)
Significance	Pathogenic
Disease	Congenital stationary night blindness not provided
Variation	info
Gene	NYX
CLNDBN	Congenital stationary night blindness, type 1A not provided
Reversed	0
HGVS	NC_000023.10:g.41332811C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012175.17, RCV000086261.1,