ADHDgene Database

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Large-scale studies

Data Summary

Published Variant
- SNP: 1391
- CNV: 398
- Others: 173
Published Gene: 359
Published Region: 128
Pathway by PBA: 8
Study: 361

SNP Report

Basic Info

Name	rs12376892 dbSNP Ensembl
Location	chr9:119348005(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	intron_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript	intron_variant(ENST00000288520; ENST00000313400; ENST00000341734; ENST00000361209; ENST00000361477; ENST00000373986; ENST00000373996) nc_transcript_variant(ENST00000423715) non_coding_exon_variant(ENST00000423715)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs12376892 (count: 0) View in gBrowse (chr9:119348005..119348005 )