rs104893786

Orientation

plus

Stabilized

plus

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

Make rs104893786(A;G)

Make rs104893786(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129528777

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893786
dbSNP (classic)	rs104893786
ClinGen	rs104893786
ebi	rs104893786
HLI	rs104893786
Exac	rs104893786
Gnomad	rs104893786
Varsome	rs104893786
LitVar	rs104893786
Map	rs104893786
PheGenI	rs104893786
Biobank	rs104893786
1000 genomes	rs104893786
hgdp	rs104893786
ensembl	rs104893786
geneview	rs104893786
scholar	rs104893786
google	rs104893786
pharmgkb	rs104893786
gwascentral	rs104893786
openSNP	rs104893786
23andMe	rs104893786
SNPshot	rs104893786
SNPdbe	rs104893786
MSV3d	rs104893786
GWAS Ctlg	rs104893786

Max Magnitude

0

OMIM	180380
Desc
Variant	0029
Related	also

ClinVar
Risk	rs104893786(G;G)
Alt	rs104893786(G;G)
Reference	Rs104893786(A;A)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4 Retinitis pigmentosa
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4 Retinitis pigmentosa
Reversed	0
HGVS	NC_000003.11:g.129247620A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013917.24, RCV000132598.1,