rs746174328

Orientation

plus

Stabilized

plus

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

Make rs746174328(-;-)

Make rs746174328(-;TA)

Make rs746174328(TA;TA)

Reference

GRCh38.p2 38.2/147

Chromosome

4

Position

16009072

Gene

PROM1

is a	snp
is	mentioned by
dbSNP	rs746174328
dbSNP (classic)	rs746174328
ClinGen	rs746174328
ebi	rs746174328
HLI	rs746174328
Exac	rs746174328
Gnomad	rs746174328
Varsome	rs746174328
LitVar	rs746174328
Map	rs746174328
PheGenI	rs746174328
Biobank	rs746174328
1000 genomes	rs746174328
hgdp	rs746174328
ensembl	rs746174328
geneview	rs746174328
scholar	rs746174328
google	rs746174328
pharmgkb	rs746174328
gwascentral	rs746174328
openSNP	rs746174328
23andMe	rs746174328
SNPshot	rs746174328
SNPdbe	rs746174328
MSV3d	rs746174328
GWAS Ctlg	rs746174328

Max Magnitude

0

ClinVar
Risk	rs746174328(-;-)
Alt	rs746174328(-;-)
Reference	Rs746174328(AT;AT)
Significance	Pathogenic
Disease	Retinitis pigmentosa 41
Variation	info
Gene	PROM1
CLNDBN	Retinitis pigmentosa 41
Reversed	0
HGVS	NC_000004.11:g.16010695_16010696delAT
CLNSRC
CLNACC	RCV000190617.1,