rs62637037

Orientation

plus

Stabilized

plus

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

Make rs62637037(A;A)

Make rs62637037(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

41474502

Gene

NYX

is a	snp
is	mentioned by
dbSNP	rs62637037
dbSNP (classic)	rs62637037
ClinGen	rs62637037
ebi	rs62637037
HLI	rs62637037
Exac	rs62637037
Gnomad	rs62637037
Varsome	rs62637037
LitVar	rs62637037
Map	rs62637037
PheGenI	rs62637037
Biobank	rs62637037
1000 genomes	rs62637037
hgdp	rs62637037
ensembl	rs62637037
geneview	rs62637037
scholar	rs62637037
google	rs62637037
pharmgkb	rs62637037
gwascentral	rs62637037
openSNP	rs62637037
23andMe	rs62637037
SNPshot	rs62637037
SNPdbe	rs62637037
MSV3d	rs62637037
GWAS Ctlg	rs62637037

Max Magnitude

0

OMIM	300278
Desc
Variant	0002
Related	also

ClinVar
Risk	rs62637037(A;A)
Alt	rs62637037(A;A)
Reference	Rs62637037(G;G)
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.41333755G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012174.11, RCV000086260.1,