rs104893789

Orientation

plus

Stabilized

plus

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

Make rs104893789(A;A)

Make rs104893789(A;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129532711

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893789
dbSNP (classic)	rs104893789
ClinGen	rs104893789
ebi	rs104893789
HLI	rs104893789
Exac	rs104893789
Gnomad	rs104893789
Varsome	rs104893789
LitVar	rs104893789
Map	rs104893789
PheGenI	rs104893789
Biobank	rs104893789
1000 genomes	rs104893789
hgdp	rs104893789
ensembl	rs104893789
geneview	rs104893789
scholar	rs104893789
google	rs104893789
pharmgkb	rs104893789
gwascentral	rs104893789
openSNP	rs104893789
23andMe	rs104893789
SNPshot	rs104893789
SNPdbe	rs104893789
MSV3d	rs104893789
GWAS Ctlg	rs104893789

Max Magnitude

0

OMIM	180380
Desc
Variant	0031
Related	also

ClinVar
Risk	rs104893789(A;A)
Alt	rs104893789(A;A)
Reference	Rs104893789(C;C)
Significance	Pathogenic
Disease	Congenital stationary night blindness
Variation	info
Gene	RHO
CLNDBN	Congenital stationary night blindness, autosomal dominant 1
Reversed	0
HGVS	NC_000003.11:g.129251554C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013919.17,