rs104893797

Orientation

plus

Stabilized

plus

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

Make rs104893797(C;G)

Make rs104893797(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129528800

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893797
dbSNP (classic)	rs104893797
ClinGen	rs104893797
ebi	rs104893797
HLI	rs104893797
Exac	rs104893797
Gnomad	rs104893797
Varsome	rs104893797
LitVar	rs104893797
Map	rs104893797
PheGenI	rs104893797
Biobank	rs104893797
1000 genomes	rs104893797
hgdp	rs104893797
ensembl	rs104893797
geneview	rs104893797
scholar	rs104893797
google	rs104893797
pharmgkb	rs104893797
gwascentral	rs104893797
openSNP	rs104893797
23andMe	rs104893797
SNPshot	rs104893797
SNPdbe	rs104893797
MSV3d	rs104893797
GWAS Ctlg	rs104893797

Max Magnitude

0

OMIM	180380
Desc
Variant	0043
Related	also

ClinVar
Risk	rs104893797(G;G)
Alt	rs104893797(G;G)
Reference	Rs104893797(C;C)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129247643C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013930.25,