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rs10922162

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs10922162(C;T)
Make rs10922162(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position197101646
GeneASPM
is asnp
is mentioned by
dbSNPrs10922162
ebirs10922162
HLIrs10922162
Exacrs10922162
Varsomers10922162
Maprs10922162
PheGenIrs10922162
hapmaprs10922162
1000 genomesrs10922162
hgdprs10922162
ensemblrs10922162
gopubmedrs10922162
geneviewrs10922162
scholarrs10922162
googlers10922162
pharmgkbrs10922162
gwascentralrs10922162
openSNPrs10922162
23andMers10922162
23andMe allrs10922162
SNP Nexus

SNPshotrs10922162
SNPdbers10922162
MSV3drs10922162
GWAS Ctlgrs10922162
GMAF0.2897
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23381943OA-icon.png]
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
Variation info
Gene ASPM
CLNDBN Primary autosomal recessive microcephaly 5 not specified
Reversed 0
HGVS NC_000001.10:g.197070776C>T
CLNSRC ClinVar GeneDx GeneReviews University of Chicago
CLNACC RCV000020793.1, RCV000145189.2,