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	rs2010506 dbSNP Ensembl
Location	chr19:19387356(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	3_prime_UTR_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000247001; ENST00000587119; ENST00000588731; ENST00000589144) nc_transcript_variant(ENST00000591007; ENST00000592188) NMD_transcript_variant(ENST00000587119; ENST00000588731; ENST00000589144) non_coding_exon_variant(ENST00000591007; ENST00000592188) upstream_gene_variant(ENST00000389363; ENST00000431465; ENST00000586064; ENST00000586107; ENST00000591001)
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 rs2010506 (count: 0) View in gBrowse (chr19:19387356..19387356 )