rs587783414

Orientation

minus

Stabilized

minus

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

Make rs587783414(-;-)

Make rs587783414(-;C)

Reference

GRCh38.p2 38.2/144

Chromosome

15

Position

48788819

Gene

CEP152

is a	snp
is	mentioned by
dbSNP	rs587783414
dbSNP (classic)	rs587783414
ClinGen	rs587783414
ebi	rs587783414
HLI	rs587783414
Exac	rs587783414
Gnomad	rs587783414
Varsome	rs587783414
LitVar	rs587783414
Map	rs587783414
PheGenI	rs587783414
Biobank	rs587783414
1000 genomes	rs587783414
hgdp	rs587783414
ensembl	rs587783414
geneview	rs587783414
scholar	rs587783414
google	rs587783414
pharmgkb	rs587783414
gwascentral	rs587783414
openSNP	rs587783414
23andMe	rs587783414
SNPshot	rs587783414
SNPdbe	rs587783414
MSV3d	rs587783414
GWAS Ctlg	rs587783414

Max Magnitude

0

ClinVar
Risk	rs587783414(-;-)
Alt	rs587783414(-;-)
Reference	Rs587783414(C;C)
Significance	Pathogenic
Disease	Primary autosomal recessive microcephaly 9
Variation	info
Gene	CEP152
CLNDBN	Primary autosomal recessive microcephaly 9
Reversed	1
HGVS	NC_000015.9:g.49081016delG
CLNSRC
CLNACC	RCV000145589.1,