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	rs3842753 dbSNP Ensembl
Location	Chr11:2181060(Fwd)
Variant Alleles	T/G
Ancestral Allele	T
Functional Annotation	3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; missense_variant; upstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000250971; ENST00000381330; ENST00000397262) NMD_transcript_variant(ENST00000356578) downstream_gene_variant(ENST00000381178; ENST00000512523; ENST00000352909; ENST00000333684; ENST00000381175) intron_variant(ENST00000356578; ENST00000381319; ENST00000397270) missense_variant(ENST00000421783) upstream_gene_variant(ENST00000481781; ENST00000476874)
No. of Studies	1 (significant: 0; non-significant: 1; trend: 0)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Nyman ES, 2007			No available information. No available information.	No evidence of association was seen. No evidence of association was seen.	Non-significant

SNP related genes (count: 4)

Literature-origin genes (count: 1)

Genes from other sources (count: 3)

Approved Symbol	Approved Name	Location
IGF2	insulin-like growth factor 2 (somatomedin A)	11p15.5
INS-IGF2	INS-IGF2 readthrough	11p15.5
INS	insulin	11p15.5

SNPs in LD with rs3842753 (count: 0) View in gBrowse (chr11:2181060..2181060 )