rs29001653

Orientation

plus

Stabilized

plus

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

Make rs29001653(A;G)

Make rs29001653(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129532722

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs29001653
dbSNP (classic)	rs29001653
ClinGen	rs29001653
ebi	rs29001653
HLI	rs29001653
Exac	rs29001653
Gnomad	rs29001653
Varsome	rs29001653
LitVar	rs29001653
Map	rs29001653
PheGenI	rs29001653
Biobank	rs29001653
1000 genomes	rs29001653
hgdp	rs29001653
ensembl	rs29001653
geneview	rs29001653
scholar	rs29001653
google	rs29001653
pharmgkb	rs29001653
gwascentral	rs29001653
openSNP	rs29001653
23andMe	rs29001653
SNPshot	rs29001653
SNPdbe	rs29001653
MSV3d	rs29001653
GWAS Ctlg	rs29001653

Max Magnitude

0

OMIM	180380
Desc	RETINITIS PIGMENTOSA 4
Variant	0016
Related	also

ClinVar
Risk	rs29001653(G;G)
Alt	rs29001653(G;G)
Reference	Rs29001653(A;A)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129251565A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013905.23,