rs267606717

Orientation

minus

Stabilized

minus

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

Make rs267606717(A;C)

Make rs267606717(C;C)

Reference

GRCh38 38.1/141

Chromosome

15

Position

48793359

Gene

CEP152

is a	snp
is	mentioned by
dbSNP	rs267606717
dbSNP (classic)	rs267606717
ClinGen	rs267606717
ebi	rs267606717
HLI	rs267606717
Exac	rs267606717
Gnomad	rs267606717
Varsome	rs267606717
LitVar	rs267606717
Map	rs267606717
PheGenI	rs267606717
Biobank	rs267606717
1000 genomes	rs267606717
hgdp	rs267606717
ensembl	rs267606717
geneview	rs267606717
scholar	rs267606717
google	rs267606717
pharmgkb	rs267606717
gwascentral	rs267606717
openSNP	rs267606717
23andMe	rs267606717
SNPshot	rs267606717
SNPdbe	rs267606717
MSV3d	rs267606717
GWAS Ctlg	rs267606717

Max Magnitude

0

ClinVar
Risk	rs267606717(C;C)
Alt	rs267606717(C;C)
Reference	Rs267606717(A;A)
Significance	Other
Disease	Primary autosomal recessive microcephaly 9 not provided
Variation	info
Gene	CEP152
CLNDBN	Primary autosomal recessive microcephaly 9 not provided
Reversed	1
HGVS	NC_000015.9:g.49085556T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000000072.5, RCV000413650.1,