rs886037612

Orientation

minus

Stabilized

minus

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

Make rs886037612(-;-)

Make rs886037612(-;G)

Reference

GRCh38.p7 38.3/149

Chromosome

4

Position

15992318

Gene

PROM1

is a	snp
is	mentioned by
dbSNP	rs886037612
dbSNP (classic)	rs886037612
ClinGen	rs886037612
ebi	rs886037612
HLI	rs886037612
Exac	rs886037612
Gnomad	rs886037612
Varsome	rs886037612
LitVar	rs886037612
Map	rs886037612
PheGenI	rs886037612
Biobank	rs886037612
1000 genomes	rs886037612
hgdp	rs886037612
ensembl	rs886037612
geneview	rs886037612
scholar	rs886037612
google	rs886037612
pharmgkb	rs886037612
gwascentral	rs886037612
openSNP	rs886037612
23andMe	rs886037612
SNPshot	rs886037612
SNPdbe	rs886037612
MSV3d	rs886037612
GWAS Ctlg	rs886037612

Max Magnitude

0

ClinVar
Risk	rs886037612(-;-)
Alt	rs886037612(-;-)
Reference	Rs886037612(G;G)
Significance	Pathogenic
Disease	Retinitis pigmentosa 41
Variation	info
Gene	PROM1
CLNDBN	Retinitis pigmentosa 41
Reversed	1
HGVS	NC_000004.11:g.15993941delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005958.3,