rs10922162

Orientation

plus

Stabilized

plus

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

Make rs10922162(C;T)

Make rs10922162(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

197101646

Gene

ASPM

is a	snp
is	mentioned by
dbSNP	rs10922162
dbSNP (classic)	rs10922162
ClinGen	rs10922162
ebi	rs10922162
HLI	rs10922162
Exac	rs10922162
Gnomad	rs10922162
Varsome	rs10922162
LitVar	rs10922162
Map	rs10922162
PheGenI	rs10922162
Biobank	rs10922162
1000 genomes	rs10922162
hgdp	rs10922162
ensembl	rs10922162
geneview	rs10922162
scholar	rs10922162
google	rs10922162
pharmgkb	rs10922162
gwascentral	rs10922162
openSNP	rs10922162
23andMe	rs10922162
SNPshot	rs10922162
SNPdbe	rs10922162
MSV3d	rs10922162
GWAS Ctlg	rs10922162

GMAF

0.2897

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 23381943]
Trait	End-stage coagulation
Title	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.
Risk Allele	C
P-val	2E-30
Odds Ratio	.52 [0.43-0.61] unit increase

ClinVar
Risk	rs10922162(T;T)
Alt	rs10922162(T;T)
Reference	Rs10922162(C;C)
Significance	Non-pathogenic
Disease	Primary autosomal recessive microcephaly 5 not specified Primary Microcephaly
Variation	info
Gene	ASPM
CLNDBN	Primary autosomal recessive microcephaly 5 not specified Primary Microcephaly, Recessive
Reversed	0
HGVS	NC_000001.10:g.197070776C>T
CLNSRC	ClinVar GeneDx GeneReviews University of Chicago
CLNACC	RCV000020793.1, RCV000145189.3, RCV000261841.1,