rs886039327

Orientation

minus

Stabilized

minus

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

Make rs886039327(C;T)

Make rs886039327(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

15

Position

48767444

Gene

CEP152

is a	snp
is	mentioned by
dbSNP	rs886039327
dbSNP (classic)	rs886039327
ClinGen	rs886039327
ebi	rs886039327
HLI	rs886039327
Exac	rs886039327
Gnomad	rs886039327
Varsome	rs886039327
LitVar	rs886039327
Map	rs886039327
PheGenI	rs886039327
Biobank	rs886039327
1000 genomes	rs886039327
hgdp	rs886039327
ensembl	rs886039327
geneview	rs886039327
scholar	rs886039327
google	rs886039327
pharmgkb	rs886039327
gwascentral	rs886039327
openSNP	rs886039327
23andMe	rs886039327
SNPshot	rs886039327
SNPdbe	rs886039327
MSV3d	rs886039327
GWAS Ctlg	rs886039327

Max Magnitude

0

ClinVar
Risk	rs886039327(T;T)
Alt	rs886039327(T;T)
Reference	Rs886039327(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CEP152
CLNDBN	not provided
Reversed	1
HGVS	NC_000015.9:g.49059641G>A
CLNSRC
CLNACC	RCV000255279.1,