rs104893779

Orientation

plus

Stabilized

plus

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

Make rs104893779(A;A)

Make rs104893779(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129532288

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893779
dbSNP (classic)	rs104893779
ClinGen	rs104893779
ebi	rs104893779
HLI	rs104893779
Exac	rs104893779
Gnomad	rs104893779
Varsome	rs104893779
LitVar	rs104893779
Map	rs104893779
PheGenI	rs104893779
Biobank	rs104893779
1000 genomes	rs104893779
hgdp	rs104893779
ensembl	rs104893779
geneview	rs104893779
scholar	rs104893779
google	rs104893779
pharmgkb	rs104893779
gwascentral	rs104893779
openSNP	rs104893779
23andMe	rs104893779
SNPshot	rs104893779
SNPdbe	rs104893779
MSV3d	rs104893779
GWAS Ctlg	rs104893779

Merged from

Rs28933992

Max Magnitude

0

OMIM	180380
Desc
Variant	0027
Related	also

OMIM	180380
Desc
Variant	0017
Related	also

ClinVar
Risk	rs104893779(A;A) rs104893779(T;T)
Alt	rs104893779(A;A) rs104893779(T;T)
Reference	Rs104893779(G;G)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129251131G>A; NC_000003.11:g.129251131G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013897.24, RCV000013915.17,