rs886037880

Orientation

minus

Stabilized

minus

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

Make rs886037880(A;A)

Make rs886037880(A;T)

Reference

GRCh38.p7 38.3/149

Chromosome

4

Position

16009093

Gene

PROM1

is a	snp
is	mentioned by
dbSNP	rs886037880
dbSNP (classic)	rs886037880
ClinGen	rs886037880
ebi	rs886037880
HLI	rs886037880
Exac	rs886037880
Gnomad	rs886037880
Varsome	rs886037880
LitVar	rs886037880
Map	rs886037880
PheGenI	rs886037880
Biobank	rs886037880
1000 genomes	rs886037880
hgdp	rs886037880
ensembl	rs886037880
geneview	rs886037880
scholar	rs886037880
google	rs886037880
pharmgkb	rs886037880
gwascentral	rs886037880
openSNP	rs886037880
23andMe	rs886037880
SNPshot	rs886037880
SNPdbe	rs886037880
MSV3d	rs886037880
GWAS Ctlg	rs886037880

Max Magnitude

0

ClinVar
Risk	rs886037880(A;A)
Alt	rs886037880(A;A)
Reference	Rs886037880(T;T)
Significance	Pathogenic
Disease	Cone-rod dystrophy 12
Variation	info
Gene	PROM1
CLNDBN	Cone-rod dystrophy 12
Reversed	1
HGVS	NC_000004.11:g.16010716A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000240342.1,