rs28933395

Orientation

plus

Stabilized

plus

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

Make rs28933395(C;G)

Make rs28933395(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129528891

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs28933395
dbSNP (classic)	rs28933395
ClinGen	rs28933395
ebi	rs28933395
HLI	rs28933395
Exac	rs28933395
Gnomad	rs28933395
Varsome	rs28933395
LitVar	rs28933395
Map	rs28933395
PheGenI	rs28933395
Biobank	rs28933395
1000 genomes	rs28933395
hgdp	rs28933395
ensembl	rs28933395
geneview	rs28933395
scholar	rs28933395
google	rs28933395
pharmgkb	rs28933395
gwascentral	rs28933395
openSNP	rs28933395
23andMe	rs28933395
SNPshot	rs28933395
SNPdbe	rs28933395
MSV3d	rs28933395
GWAS Ctlg	rs28933395

Max Magnitude

0

OMIM	180380
Desc	RETINITIS PIGMENTOSA 4
Variant	0024
Related	also

ClinVar
Risk	rs28933395(G;G)
Alt	rs28933395(G;G)
Reference	Rs28933395(C;C)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129247734C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013912.24,