rs876657718

Orientation

plus

Stabilized

plus

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

Make rs876657718(A;A)

Make rs876657718(A;C)

Reference

GRCh38.p2 38.2/147

Chromosome

4

Position

625917

Gene

PDE6B

is a	snp
is	mentioned by
dbSNP	rs876657718
dbSNP (classic)	rs876657718
ClinGen	rs876657718
ebi	rs876657718
HLI	rs876657718
Exac	rs876657718
Gnomad	rs876657718
Varsome	rs876657718
LitVar	rs876657718
Map	rs876657718
PheGenI	rs876657718
Biobank	rs876657718
1000 genomes	rs876657718
hgdp	rs876657718
ensembl	rs876657718
geneview	rs876657718
scholar	rs876657718
google	rs876657718
pharmgkb	rs876657718
gwascentral	rs876657718
openSNP	rs876657718
23andMe	rs876657718
SNPshot	rs876657718
SNPdbe	rs876657718
MSV3d	rs876657718
GWAS Ctlg	rs876657718

Max Magnitude

0

ClinVar
Risk	rs876657718(A;A)
Alt	rs876657718(A;A)
Reference	Rs876657718(C;C)
Significance	Pathogenic
Disease	Retinitis pigmentosa Retinal dystrophy
Variation	info
Gene	PDE6B
CLNDBN	Retinitis pigmentosa Retinal dystrophy
Reversed	0
HGVS	NC_000004.11:g.619706C>A
CLNSRC
CLNACC	RCV000220232.1, RCV000225461.1,