rs104893776

Orientation

plus

Stabilized

plus

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

Make rs104893776(A;G)

Make rs104893776(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129532253

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893776
dbSNP (classic)	rs104893776
ClinGen	rs104893776
ebi	rs104893776
HLI	rs104893776
Exac	rs104893776
Gnomad	rs104893776
Varsome	rs104893776
LitVar	rs104893776
Map	rs104893776
PheGenI	rs104893776
Biobank	rs104893776
1000 genomes	rs104893776
hgdp	rs104893776
ensembl	rs104893776
geneview	rs104893776
scholar	rs104893776
google	rs104893776
pharmgkb	rs104893776
gwascentral	rs104893776
openSNP	rs104893776
23andMe	rs104893776
SNPshot	rs104893776
SNPdbe	rs104893776
MSV3d	rs104893776
GWAS Ctlg	rs104893776

Max Magnitude

0

OMIM	180380
Desc
Variant	0013
Related	also

ClinVar
Risk	rs104893776(G;G)
Alt	rs104893776(G;G)
Reference	Rs104893776(A;A)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129251096A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013899.24,