rs1060499758

Orientation

minus

Stabilized

minus

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

Make rs1060499758(A;A)

Make rs1060499758(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

197094079

Gene

ASPM

is a	snp
is	mentioned by
dbSNP	rs1060499758
dbSNP (classic)	rs1060499758
ClinGen	rs1060499758
ebi	rs1060499758
HLI	rs1060499758
Exac	rs1060499758
Gnomad	rs1060499758
Varsome	rs1060499758
LitVar	rs1060499758
Map	rs1060499758
PheGenI	rs1060499758
Biobank	rs1060499758
1000 genomes	rs1060499758
hgdp	rs1060499758
ensembl	rs1060499758
geneview	rs1060499758
scholar	rs1060499758
google	rs1060499758
pharmgkb	rs1060499758
gwascentral	rs1060499758
openSNP	rs1060499758
23andMe	rs1060499758
SNPshot	rs1060499758
SNPdbe	rs1060499758
MSV3d	rs1060499758
GWAS Ctlg	rs1060499758

Max Magnitude

0

ClinVar
Risk	rs1060499758(A;A)
Alt	rs1060499758(A;A)
Reference	Rs1060499758(G;G)
Significance	Probable-Pathogenic
Disease	Microcephaly
Variation	info
Gene	ASPM
CLNDBN	Microcephaly
Reversed	1
HGVS	NC_000001.10:g.197063209C>T
CLNSRC
CLNACC	RCV000454144.1,