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	rs13021295 dbSNP Ensembl
Location	chr2:225811581(Fwd)
Variant Alleles	T/A
Ancestral Allele	T
Functional Annotation	intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant. Polyphen Annotation: benign(ENST00000409592) SIFT Annotation: tolerated(ENST00000409592)
Consequence to Transcript	intron_variant(ENST00000258390; ENST00000435582; ENST00000471810; ENST00000492369) missense_variant(ENST00000409592) nc_transcript_variant(ENST00000471810; ENST00000474102; ENST00000492369) NMD_transcript_variant(ENST00000435582) non_coding_exon_variant(ENST00000474102)
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 rs13021295 (count: 0) View in gBrowse (chr2:225811581..225811581 )