rs878853328

Orientation

plus

Stabilized

plus

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

Make rs878853328(C;T)

Make rs878853328(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

8

Position

54625914

Gene

RP1

is a	snp
is	mentioned by
dbSNP	rs878853328
dbSNP (classic)	rs878853328
ClinGen	rs878853328
ebi	rs878853328
HLI	rs878853328
Exac	rs878853328
Gnomad	rs878853328
Varsome	rs878853328
LitVar	rs878853328
Map	rs878853328
PheGenI	rs878853328
Biobank	rs878853328
1000 genomes	rs878853328
hgdp	rs878853328
ensembl	rs878853328
geneview	rs878853328
scholar	rs878853328
google	rs878853328
pharmgkb	rs878853328
gwascentral	rs878853328
openSNP	rs878853328
23andMe	rs878853328
SNPshot	rs878853328
SNPdbe	rs878853328
MSV3d	rs878853328
GWAS Ctlg	rs878853328

Max Magnitude

0

ClinVar
Risk	rs878853328(T;T)
Alt	rs878853328(T;T)
Reference	Rs878853328(C;C)
Significance	Probable-Pathogenic
Disease	Retinal dystrophy
Variation	info
Gene	RP1
CLNDBN	Retinal dystrophy
Reversed	0
HGVS	NC_000008.10:g.55538474C>T
CLNSRC
CLNACC	RCV000225475.1,