rs886037881

Orientation

minus

Stabilized

minus

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

Make rs886037881(-;-)

Make rs886037881(-;GTTTCCCTGT)

Make rs886037881(GTTTCCCTGT;GTTTCCCTGT)

Reference

GRCh38.p7 38.3/149

Chromosome

4

Position

15984372

Gene

PROM1

is a	snp
is	mentioned by
dbSNP	rs886037881
dbSNP (classic)	rs886037881
ClinGen	rs886037881
ebi	rs886037881
HLI	rs886037881
Exac	rs886037881
Gnomad	rs886037881
Varsome	rs886037881
LitVar	rs886037881
Map	rs886037881
PheGenI	rs886037881
Biobank	rs886037881
1000 genomes	rs886037881
hgdp	rs886037881
ensembl	rs886037881
geneview	rs886037881
scholar	rs886037881
google	rs886037881
pharmgkb	rs886037881
gwascentral	rs886037881
openSNP	rs886037881
23andMe	rs886037881
SNPshot	rs886037881
SNPdbe	rs886037881
MSV3d	rs886037881
GWAS Ctlg	rs886037881

Max Magnitude

0

ClinVar
Risk	rs886037881(-;-)
Alt	rs886037881(-;-)
Reference	Rs886037881(CTGTGTTTCC;CTGTGTTTCC)
Significance	Pathogenic
Disease	Cone-rod dystrophy 12
Variation	info
Gene	PROM1
CLNDBN	Cone-rod dystrophy 12
Reversed	1
HGVS	NC_000004.11:g.15985995_15986004delACAGGGAAAC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000239774.1,