rs878853400

Orientation

minus

Stabilized

minus

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

Make rs878853400(-;-)

Make rs878853400(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

4

Position

15984327

Gene

PROM1

is a	snp
is	mentioned by
dbSNP	rs878853400
dbSNP (classic)	rs878853400
ClinGen	rs878853400
ebi	rs878853400
HLI	rs878853400
Exac	rs878853400
Gnomad	rs878853400
Varsome	rs878853400
LitVar	rs878853400
Map	rs878853400
PheGenI	rs878853400
Biobank	rs878853400
1000 genomes	rs878853400
hgdp	rs878853400
ensembl	rs878853400
geneview	rs878853400
scholar	rs878853400
google	rs878853400
pharmgkb	rs878853400
gwascentral	rs878853400
openSNP	rs878853400
23andMe	rs878853400
SNPshot	rs878853400
SNPdbe	rs878853400
MSV3d	rs878853400
GWAS Ctlg	rs878853400

Max Magnitude

0

ClinVar
Risk	rs878853400(-;-)
Alt	rs878853400(-;-)
Reference	Rs878853400(C;C)
Significance	Probable-Pathogenic
Disease	Retinal dystrophy
Variation	info
Gene	PROM1
CLNDBN	Retinal dystrophy
Reversed	1
HGVS	NC_000004.11:g.15985950delG
CLNSRC
CLNACC	RCV000225433.1,