rs527236101

Orientation

plus

Stabilized

plus

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

Make rs527236101(A;A)

Make rs527236101(A;C)

Reference

GRCh38 38.1/142

Chromosome

3

Position

129528913

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs527236101
dbSNP (classic)	rs527236101
ClinGen	rs527236101
ebi	rs527236101
HLI	rs527236101
Exac	rs527236101
Gnomad	rs527236101
Varsome	rs527236101
LitVar	rs527236101
Map	rs527236101
PheGenI	rs527236101
Biobank	rs527236101
1000 genomes	rs527236101
hgdp	rs527236101
ensembl	rs527236101
geneview	rs527236101
scholar	rs527236101
google	rs527236101
pharmgkb	rs527236101
gwascentral	rs527236101
openSNP	rs527236101
23andMe	rs527236101
SNPshot	rs527236101
SNPdbe	rs527236101
MSV3d	rs527236101
GWAS Ctlg	rs527236101

Max Magnitude

0

ClinVar
Risk	rs527236101(A;A)
Alt	rs527236101(A;A)
Reference	Rs527236101(C;C)
Significance	Probable-Pathogenic
Disease	Retinitis pigmentosa
Variation	info
Gene	RHO
CLNDBN	Retinitis pigmentosa
Reversed	0
HGVS	NC_000003.11:g.129247756C>A
CLNSRC	ClinVar
CLNACC	RCV000132596.1,