rs104893778

Orientation

plus

Stabilized

plus

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

Make rs104893778(C;T)

Make rs104893778(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129533701

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893778
dbSNP (classic)	rs104893778
ClinGen	rs104893778
ebi	rs104893778
HLI	rs104893778
Exac	rs104893778
Gnomad	rs104893778
Varsome	rs104893778
LitVar	rs104893778
Map	rs104893778
PheGenI	rs104893778
Biobank	rs104893778
1000 genomes	rs104893778
hgdp	rs104893778
ensembl	rs104893778
geneview	rs104893778
scholar	rs104893778
google	rs104893778
pharmgkb	rs104893778
gwascentral	rs104893778
openSNP	rs104893778
23andMe	rs104893778
SNPshot	rs104893778
SNPdbe	rs104893778
MSV3d	rs104893778
GWAS Ctlg	rs104893778

Max Magnitude

0

OMIM	180380
Desc
Variant	0015
Related	also

ClinVar
Risk	rs104893778(T;T)
Alt	rs104893778(T;T)
Reference	Rs104893778(C;C)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129252544C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013904.17,