rs104893792

Orientation

plus

Stabilized

plus

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

Make rs104893792(C;C)

Make rs104893792(C;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129528884

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893792
dbSNP (classic)	rs104893792
ClinGen	rs104893792
ebi	rs104893792
HLI	rs104893792
Exac	rs104893792
Gnomad	rs104893792
Varsome	rs104893792
LitVar	rs104893792
Map	rs104893792
PheGenI	rs104893792
Biobank	rs104893792
1000 genomes	rs104893792
hgdp	rs104893792
ensembl	rs104893792
geneview	rs104893792
scholar	rs104893792
google	rs104893792
pharmgkb	rs104893792
gwascentral	rs104893792
openSNP	rs104893792
23andMe	rs104893792
SNPshot	rs104893792
SNPdbe	rs104893792
MSV3d	rs104893792
GWAS Ctlg	rs104893792

Max Magnitude

0

OMIM	180380
Desc
Variant	0034
Related	also

ClinVar
Risk	rs104893792(C;C)
Alt	rs104893792(C;C)
Reference	Rs104893792(G;G)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129247727G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013922.23,