rs29001637

Orientation

plus

Stabilized

plus

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

Make rs29001637(C;T)

Make rs29001637(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129533710

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs29001637
dbSNP (classic)	rs29001637
ClinGen	rs29001637
ebi	rs29001637
HLI	rs29001637
Exac	rs29001637
Gnomad	rs29001637
Varsome	rs29001637
LitVar	rs29001637
Map	rs29001637
PheGenI	rs29001637
Biobank	rs29001637
1000 genomes	rs29001637
hgdp	rs29001637
ensembl	rs29001637
geneview	rs29001637
scholar	rs29001637
google	rs29001637
pharmgkb	rs29001637
gwascentral	rs29001637
openSNP	rs29001637
23andMe	rs29001637
SNPshot	rs29001637
SNPdbe	rs29001637
MSV3d	rs29001637
GWAS Ctlg	rs29001637

Max Magnitude

0

OMIM	180380
Desc	RETINITIS PIGMENTOSA 4
Variant	0003
Related	also

ClinVar
Risk	rs29001637(T;T)
Alt	rs29001637(T;T)
Reference	Rs29001637(C;C)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129252553C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013889.24,