rs104893780

Orientation

plus

Stabilized

plus

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

Make rs104893780(A;A)

Make rs104893780(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129532264

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893780
dbSNP (classic)	rs104893780
ClinGen	rs104893780
ebi	rs104893780
HLI	rs104893780
Exac	rs104893780
Gnomad	rs104893780
Varsome	rs104893780
LitVar	rs104893780
Map	rs104893780
PheGenI	rs104893780
Biobank	rs104893780
1000 genomes	rs104893780
hgdp	rs104893780
ensembl	rs104893780
geneview	rs104893780
scholar	rs104893780
google	rs104893780
pharmgkb	rs104893780
gwascentral	rs104893780
openSNP	rs104893780
23andMe	rs104893780
SNPshot	rs104893780
SNPdbe	rs104893780
MSV3d	rs104893780
GWAS Ctlg	rs104893780

Max Magnitude

0

OMIM	180380
Desc
Variant	0021
Related	also

ClinVar
Risk	rs104893780(A;A)
Alt	rs104893780(A;A)
Reference	Rs104893780(G;G)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129251107G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013908.17,