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rs7192086

From SNPedia

Orientationplus
Stabilizedplus
Make rs7192086(A;A)
Make rs7192086(A;T)
Make rs7192086(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position12967754
GeneSHISA9
is asnp
is mentioned by
dbSNPrs7192086
ebirs7192086
HLIrs7192086
Exacrs7192086
Varsomers7192086
Maprs7192086
PheGenIrs7192086
hapmaprs7192086
1000 genomesrs7192086
hgdprs7192086
ensemblrs7192086
gopubmedrs7192086
geneviewrs7192086
scholarrs7192086
googlers7192086
pharmgkbrs7192086
gwascentralrs7192086
openSNPrs7192086
23andMers7192086
23andMe allrs7192086
SNP Nexus

SNPshotrs7192086
SNPdbers7192086
MSV3drs7192086
GWAS Ctlgrs7192086
GMAF0.2241
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS
SNP rs7192086
PubMedID [PMID 18677311]
Condition Schizophrenia
Gene Intergenic
Risk Allele T
pValue 6.00E-006
OR 1.12
95% CI



OMIM606158
DescBSCL2 GENE; BSCL2
Variant
Relatedalso
[PMID 19396477OA-icon.png] A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier?


GET Evidence
rs7192086
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.741379
summary



[PMID 22005930OA-icon.png] Genome-wide association study of Alzheimer's disease with psychotic symptoms.