rs104893771

Orientation

plus

Stabilized

plus

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

Make rs104893771(A;A)

Make rs104893771(A;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

129528993

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs104893771
dbSNP (classic)	rs104893771
ClinGen	rs104893771
ebi	rs104893771
HLI	rs104893771
Exac	rs104893771
Gnomad	rs104893771
Varsome	rs104893771
LitVar	rs104893771
Map	rs104893771
PheGenI	rs104893771
Biobank	rs104893771
1000 genomes	rs104893771
hgdp	rs104893771
ensembl	rs104893771
geneview	rs104893771
scholar	rs104893771
google	rs104893771
pharmgkb	rs104893771
gwascentral	rs104893771
openSNP	rs104893771
23andMe	rs104893771
SNPshot	rs104893771
SNPdbe	rs104893771
MSV3d	rs104893771
GWAS Ctlg	rs104893771

Max Magnitude

0

OMIM	180380
Desc
Variant	0008
Related	also

ClinVar
Risk	rs104893771(A;A)
Alt	rs104893771(A;A)
Reference	Rs104893771(T;T)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4
Reversed	0
HGVS	NC_000003.11:g.129247836T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013894.24,