rs104893769

Orientation

plus

Stabilized

plus

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

Make rs104893769(C;T)

Make rs104893769(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129528783

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893769
dbSNP (classic)	rs104893769
ClinGen	rs104893769
ebi	rs104893769
HLI	rs104893769
Exac	rs104893769
Gnomad	rs104893769
Varsome	rs104893769
LitVar	rs104893769
Map	rs104893769
PheGenI	rs104893769
Biobank	rs104893769
1000 genomes	rs104893769
hgdp	rs104893769
ensembl	rs104893769
geneview	rs104893769
scholar	rs104893769
google	rs104893769
pharmgkb	rs104893769
gwascentral	rs104893769
openSNP	rs104893769
23andMe	rs104893769
SNPshot	rs104893769
SNPdbe	rs104893769
MSV3d	rs104893769
GWAS Ctlg	rs104893769

Max Magnitude

0

OMIM	180380
Desc
Variant	0006
Related	also

ClinVar
Risk	rs104893769(T;T)
Alt	rs104893769(T;T)
Reference	Rs104893769(C;C)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129247626C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013892.24,