rs104893788

Orientation

plus

Stabilized

plus

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

Make rs104893788(A;A)

Make rs104893788(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129529074

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893788
dbSNP (classic)	rs104893788
ClinGen	rs104893788
ebi	rs104893788
HLI	rs104893788
Exac	rs104893788
Gnomad	rs104893788
Varsome	rs104893788
LitVar	rs104893788
Map	rs104893788
PheGenI	rs104893788
Biobank	rs104893788
1000 genomes	rs104893788
hgdp	rs104893788
ensembl	rs104893788
geneview	rs104893788
scholar	rs104893788
google	rs104893788
pharmgkb	rs104893788
gwascentral	rs104893788
openSNP	rs104893788
23andMe	rs104893788
SNPshot	rs104893788
SNPdbe	rs104893788
MSV3d	rs104893788
GWAS Ctlg	rs104893788

Max Magnitude

0

OMIM	180380
Desc
Variant	0036
Related	also

ClinVar
Risk	rs104893788(A;A) rs104893788(C;C)
Alt	rs104893788(A;A) rs104893788(C;C)
Reference	Rs104893788(G;G)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129247917G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013923.24,