rs104894459

Orientation

minus

Stabilized

minus

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

Make rs104894459(A;A)

Make rs104894459(A;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

24082701

Gene

NRL

is a	snp
is	mentioned by
dbSNP	rs104894459
dbSNP (classic)	rs104894459
ClinGen	rs104894459
ebi	rs104894459
HLI	rs104894459
Exac	rs104894459
Gnomad	rs104894459
Varsome	rs104894459
LitVar	rs104894459
Map	rs104894459
PheGenI	rs104894459
Biobank	rs104894459
1000 genomes	rs104894459
hgdp	rs104894459
ensembl	rs104894459
geneview	rs104894459
scholar	rs104894459
google	rs104894459
pharmgkb	rs104894459
gwascentral	rs104894459
openSNP	rs104894459
23andMe	rs104894459
SNPshot	rs104894459
SNPdbe	rs104894459
MSV3d	rs104894459
GWAS Ctlg	rs104894459

Max Magnitude

0

OMIM	162080
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894459(A;A)
Alt	rs104894459(A;A)
Reference	Rs104894459(T;T)
Significance	Pathogenic
Disease	Retinitis pigmentosa 27
Variation	info
Gene	NRL
CLNDBN	Retinitis pigmentosa 27
Reversed	1
HGVS	NC_000014.8:g.24551910A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015086.22,