ADHDgene Database

Hot Results

Quick Search

Keyword:
Type:

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	rs7895872 dbSNP Ensembl
Location	chr10:112678657(Fwd)
Variant Alleles	G/T
Ancestral Allele	G
Functional Annotation	5_prime_UTR_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript	5_prime_UTR_variant(ENST00000605742) intron_variant(ENST00000398289; ENST00000422050; ENST00000423273; ENST00000431847; ENST00000436562; ENST00000447005; ENST00000448814; ENST00000454061) nc_transcript_variant(ENST00000422050; ENST00000431847) NMD_transcript_variant(ENST00000398289) upstream_gene_variant(ENST00000265277; ENST00000369452; ENST00000480155; ENST00000489390; ENST00000489783)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Literature-origin genes (count: 0)

Genes from other sources (count: 2)

SNPs in LD with rs7895872 (count: 0) View in gBrowse (chr10:112678657..112678657 )