rs104893768

Orientation

plus

Stabilized

plus

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

Make rs104893768(A;A)

Make rs104893768(A;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129528801

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893768
dbSNP (classic)	rs104893768
ClinGen	rs104893768
ebi	rs104893768
HLI	rs104893768
Exac	rs104893768
Gnomad	rs104893768
Varsome	rs104893768
LitVar	rs104893768
Map	rs104893768
PheGenI	rs104893768
Biobank	rs104893768
1000 genomes	rs104893768
hgdp	rs104893768
ensembl	rs104893768
geneview	rs104893768
scholar	rs104893768
google	rs104893768
pharmgkb	rs104893768
gwascentral	rs104893768
openSNP	rs104893768
23andMe	rs104893768
SNPshot	rs104893768
SNPdbe	rs104893768
MSV3d	rs104893768
GWAS Ctlg	rs104893768

Max Magnitude

0

OMIM	180380
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104893768(A;A)
Alt	rs104893768(A;A)
Reference	Rs104893768(C;C)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4 not provided
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4 not provided
Reversed	0
HGVS	NC_000003.11:g.129247644C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013887.17, RCV000490234.1,