rs398122977

Orientation

minus

Stabilized

minus

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

Make rs398122977(C;C)

Make rs398122977(C;T)

Reference

GRCh38 38.1/141

Chromosome

15

Position

48756099

Gene

CEP152

is a	snp
is	mentioned by
dbSNP	rs398122977
dbSNP (classic)	rs398122977
ClinGen	rs398122977
ebi	rs398122977
HLI	rs398122977
Exac	rs398122977
Gnomad	rs398122977
Varsome	rs398122977
LitVar	rs398122977
Map	rs398122977
PheGenI	rs398122977
Biobank	rs398122977
1000 genomes	rs398122977
hgdp	rs398122977
ensembl	rs398122977
geneview	rs398122977
scholar	rs398122977
google	rs398122977
pharmgkb	rs398122977
gwascentral	rs398122977
openSNP	rs398122977
23andMe	rs398122977
SNPshot	rs398122977
SNPdbe	rs398122977
MSV3d	rs398122977
GWAS Ctlg	rs398122977

Max Magnitude

0

ClinVar
Risk	rs398122977(C;C)
Alt	rs398122977(C;C)
Reference	Rs398122977(T;T)
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.49048296A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000077752.5,