rs878853327

Orientation

plus

Stabilized

plus

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

Make rs878853327(-;-)

Make rs878853327(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

8

Position

54625344

Gene

RP1

is a	snp
is	mentioned by
dbSNP	rs878853327
dbSNP (classic)	rs878853327
ClinGen	rs878853327
ebi	rs878853327
HLI	rs878853327
Exac	rs878853327
Gnomad	rs878853327
Varsome	rs878853327
LitVar	rs878853327
Map	rs878853327
PheGenI	rs878853327
Biobank	rs878853327
1000 genomes	rs878853327
hgdp	rs878853327
ensembl	rs878853327
geneview	rs878853327
scholar	rs878853327
google	rs878853327
pharmgkb	rs878853327
gwascentral	rs878853327
openSNP	rs878853327
23andMe	rs878853327
SNPshot	rs878853327
SNPdbe	rs878853327
MSV3d	rs878853327
GWAS Ctlg	rs878853327

Max Magnitude

0

ClinVar
Risk	rs878853327(-;-)
Alt	rs878853327(-;-)
Reference	Rs878853327(G;G)
Significance	Probable-Pathogenic
Disease	Retinal dystrophy
Variation	info
Gene	RP1
CLNDBN	Retinal dystrophy
Reversed	0
HGVS	NC_000008.10:g.55537904delG
CLNSRC
CLNACC	RCV000225399.1,