rs104893772

Orientation

plus

Stabilized

plus

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

Make rs104893772(A;A)

Make rs104893772(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129528999

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893772
dbSNP (classic)	rs104893772
ClinGen	rs104893772
ebi	rs104893772
HLI	rs104893772
Exac	rs104893772
Gnomad	rs104893772
Varsome	rs104893772
LitVar	rs104893772
Map	rs104893772
PheGenI	rs104893772
Biobank	rs104893772
1000 genomes	rs104893772
hgdp	rs104893772
ensembl	rs104893772
geneview	rs104893772
scholar	rs104893772
google	rs104893772
pharmgkb	rs104893772
gwascentral	rs104893772
openSNP	rs104893772
23andMe	rs104893772
SNPshot	rs104893772
SNPdbe	rs104893772
MSV3d	rs104893772
GWAS Ctlg	rs104893772

Max Magnitude

0

OMIM	180380
Desc
Variant	0009
Related	also

ClinVar
Risk	rs104893772(A;A)
Alt	rs104893772(A;A)
Reference	Rs104893772(G;G)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129247842G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013895.17,