rs766246531

Orientation

plus

Stabilized

plus

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

Make rs766246531(-;-)

Make rs766246531(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

16025200

Gene

PROM1

is a	snp
is	mentioned by
dbSNP	rs766246531
dbSNP (classic)	rs766246531
ClinGen	rs766246531
ebi	rs766246531
HLI	rs766246531
Exac	rs766246531
Gnomad	rs766246531
Varsome	rs766246531
LitVar	rs766246531
Map	rs766246531
PheGenI	rs766246531
Biobank	rs766246531
1000 genomes	rs766246531
hgdp	rs766246531
ensembl	rs766246531
geneview	rs766246531
scholar	rs766246531
google	rs766246531
pharmgkb	rs766246531
gwascentral	rs766246531
openSNP	rs766246531
23andMe	rs766246531
SNPshot	rs766246531
SNPdbe	rs766246531
MSV3d	rs766246531
GWAS Ctlg	rs766246531

Max Magnitude

0

ClinVar
Risk	rs766246531(-;-)
Alt	rs766246531(-;-)
Reference	Rs766246531(T;T)
Significance	Probable-Pathogenic
Disease	Retinitis pigmentosa 41
Variation	info
Gene	PROM1
CLNDBN	Retinitis pigmentosa 41
Reversed	0
HGVS	NC_000004.11:g.16026823delT
CLNSRC
CLNACC	RCV000454283.1,