rs876661154

Orientation

minus

Stabilized

minus

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

Make rs876661154(-;-)

Make rs876661154(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

197100652

Gene

ASPM

is a	snp
is	mentioned by
dbSNP	rs876661154
dbSNP (classic)	rs876661154
ClinGen	rs876661154
ebi	rs876661154
HLI	rs876661154
Exac	rs876661154
Gnomad	rs876661154
Varsome	rs876661154
LitVar	rs876661154
Map	rs876661154
PheGenI	rs876661154
Biobank	rs876661154
1000 genomes	rs876661154
hgdp	rs876661154
ensembl	rs876661154
geneview	rs876661154
scholar	rs876661154
google	rs876661154
pharmgkb	rs876661154
gwascentral	rs876661154
openSNP	rs876661154
23andMe	rs876661154
SNPshot	rs876661154
SNPdbe	rs876661154
MSV3d	rs876661154
GWAS Ctlg	rs876661154

Max Magnitude

0

ClinVar
Risk	rs876661154(-;-)
Alt	rs876661154(-;-)
Reference	Rs876661154(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ASPM
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.197069782delG
CLNSRC
CLNACC	RCV000222135.1,