rs753406334

Orientation

plus

Stabilized

plus

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

Make rs753406334(C;C)

Make rs753406334(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

197104519

Gene

ASPM

is a	snp
is	mentioned by
dbSNP	rs753406334
dbSNP (classic)	rs753406334
ClinGen	rs753406334
ebi	rs753406334
HLI	rs753406334
Exac	rs753406334
Gnomad	rs753406334
Varsome	rs753406334
LitVar	rs753406334
Map	rs753406334
PheGenI	rs753406334
Biobank	rs753406334
1000 genomes	rs753406334
hgdp	rs753406334
ensembl	rs753406334
geneview	rs753406334
scholar	rs753406334
google	rs753406334
pharmgkb	rs753406334
gwascentral	rs753406334
openSNP	rs753406334
23andMe	rs753406334
SNPshot	rs753406334
SNPdbe	rs753406334
MSV3d	rs753406334
GWAS Ctlg	rs753406334

Max Magnitude

0

ClinVar
Risk	rs753406334(A;A) rs753406334(C;C)
Alt	rs753406334(A;A) rs753406334(C;C)
Reference	Rs753406334(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ASPM
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.197073649G>A
CLNSRC
CLNACC	RCV000220667.2,