rs104893777

Orientation

plus

Stabilized

plus

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

Make rs104893777(A;G)

Make rs104893777(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129532289

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893777
dbSNP (classic)	rs104893777
ClinGen	rs104893777
ebi	rs104893777
HLI	rs104893777
Exac	rs104893777
Gnomad	rs104893777
Varsome	rs104893777
LitVar	rs104893777
Map	rs104893777
PheGenI	rs104893777
Biobank	rs104893777
1000 genomes	rs104893777
hgdp	rs104893777
ensembl	rs104893777
geneview	rs104893777
scholar	rs104893777
google	rs104893777
pharmgkb	rs104893777
gwascentral	rs104893777
openSNP	rs104893777
23andMe	rs104893777
SNPshot	rs104893777
SNPdbe	rs104893777
MSV3d	rs104893777
GWAS Ctlg	rs104893777

Max Magnitude

0

OMIM	180380
Desc
Variant	0014
Related	also

ClinVar
Risk	rs104893777(G;G)
Alt	rs104893777(G;G)
Reference	Rs104893777(A;A)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129251132A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013900.23,