rs104893782

Orientation

plus

Stabilized

plus

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

Make rs104893782(G;G)

Make rs104893782(G;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129532340

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893782
dbSNP (classic)	rs104893782
ClinGen	rs104893782
ebi	rs104893782
HLI	rs104893782
Exac	rs104893782
Gnomad	rs104893782
Varsome	rs104893782
LitVar	rs104893782
Map	rs104893782
PheGenI	rs104893782
Biobank	rs104893782
1000 genomes	rs104893782
hgdp	rs104893782
ensembl	rs104893782
geneview	rs104893782
scholar	rs104893782
google	rs104893782
pharmgkb	rs104893782
gwascentral	rs104893782
openSNP	rs104893782
23andMe	rs104893782
SNPshot	rs104893782
SNPdbe	rs104893782
MSV3d	rs104893782
GWAS Ctlg	rs104893782

Merged from

Rs28933995

Max Magnitude

0

OMIM	180380
Desc
Variant	0030
Related	also

OMIM	180380
Desc
Variant	0028
Related	also

ClinVar
Risk	rs104893782(G;G)
Alt	rs104893782(G;G)
Reference	Rs104893782(T;T)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129251183T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013918.23,