rs104893774

Orientation

plus

Stabilized

plus

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

Make rs104893774(G;T)

Make rs104893774(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129530918

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893774
dbSNP (classic)	rs104893774
ClinGen	rs104893774
ebi	rs104893774
HLI	rs104893774
Exac	rs104893774
Gnomad	rs104893774
Varsome	rs104893774
LitVar	rs104893774
Map	rs104893774
PheGenI	rs104893774
Biobank	rs104893774
1000 genomes	rs104893774
hgdp	rs104893774
ensembl	rs104893774
geneview	rs104893774
scholar	rs104893774
google	rs104893774
pharmgkb	rs104893774
gwascentral	rs104893774
openSNP	rs104893774
23andMe	rs104893774
SNPshot	rs104893774
SNPdbe	rs104893774
MSV3d	rs104893774
GWAS Ctlg	rs104893774

Max Magnitude

0

OMIM	180380
Desc
Variant	0011
Related	also

ClinVar
Risk	rs104893774(A;A) rs104893774(T;T)
Alt	rs104893774(A;A) rs104893774(T;T)
Reference	Rs104893774(G;G)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4 not provided
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4 not provided
Reversed	0
HGVS	NC_000003.11:g.129249761G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013898.24, RCV000256085.1,