rs104893773

Orientation

plus

Stabilized

plus

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

Make rs104893773(G;T)

Make rs104893773(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129529049

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893773
dbSNP (classic)	rs104893773
ClinGen	rs104893773
ebi	rs104893773
HLI	rs104893773
Exac	rs104893773
Gnomad	rs104893773
Varsome	rs104893773
LitVar	rs104893773
Map	rs104893773
PheGenI	rs104893773
Biobank	rs104893773
1000 genomes	rs104893773
hgdp	rs104893773
ensembl	rs104893773
geneview	rs104893773
scholar	rs104893773
google	rs104893773
pharmgkb	rs104893773
gwascentral	rs104893773
openSNP	rs104893773
23andMe	rs104893773
SNPshot	rs104893773
SNPdbe	rs104893773
MSV3d	rs104893773
GWAS Ctlg	rs104893773

Merged from

Rs28933994

Max Magnitude

0

OMIM	180380
Desc
Variant	0025
Related	also

OMIM	180380
Desc
Variant	0010
Related	also

ClinVar
Risk	rs104893773(A;A) rs104893773(T;T)
Alt	rs104893773(A;A) rs104893773(T;T)
Reference	Rs104893773(G;G)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129247892G>A; NC_000003.11:g.129247892G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013913.24, RCV000013896.23,