rs104893787

Orientation

plus

Stabilized

plus

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

Make rs104893787(A;A)

Make rs104893787(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129529062

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893787
dbSNP (classic)	rs104893787
ClinGen	rs104893787
ebi	rs104893787
HLI	rs104893787
Exac	rs104893787
Gnomad	rs104893787
Varsome	rs104893787
LitVar	rs104893787
Map	rs104893787
PheGenI	rs104893787
Biobank	rs104893787
1000 genomes	rs104893787
hgdp	rs104893787
ensembl	rs104893787
geneview	rs104893787
scholar	rs104893787
google	rs104893787
pharmgkb	rs104893787
gwascentral	rs104893787
openSNP	rs104893787
23andMe	rs104893787
SNPshot	rs104893787
SNPdbe	rs104893787
MSV3d	rs104893787
GWAS Ctlg	rs104893787

Max Magnitude

0

OMIM	180380
Desc
Variant	0035
Related	also

ClinVar
Risk	rs104893787(A;A)
Alt	rs104893787(A;A)
Reference	Rs104893787(G;G)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129247905G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013910.24,