rs869320618

Orientation

plus

Stabilized

plus

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

Make rs869320618(A;A)

Make rs869320618(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

129530996

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs869320618
dbSNP (classic)	rs869320618
ClinGen	rs869320618
ebi	rs869320618
HLI	rs869320618
Exac	rs869320618
Gnomad	rs869320618
Varsome	rs869320618
LitVar	rs869320618
Map	rs869320618
PheGenI	rs869320618
Biobank	rs869320618
1000 genomes	rs869320618
hgdp	rs869320618
ensembl	rs869320618
geneview	rs869320618
scholar	rs869320618
google	rs869320618
pharmgkb	rs869320618
gwascentral	rs869320618
openSNP	rs869320618
23andMe	rs869320618
SNPshot	rs869320618
SNPdbe	rs869320618
MSV3d	rs869320618
GWAS Ctlg	rs869320618

Max Magnitude

0

ClinVar
Risk	rs869320618(A;A)
Alt	rs869320618(A;A)
Reference	Rs869320618(G;G)
Significance	Pathogenic
Disease	Retinitis pigmentosa 4
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa 4, autosomal recessive
Reversed	0
HGVS	NC_000003.11:g.129249839G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000022756.25,