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	rs10849949 dbSNP Ensembl
Location	chr12:111893537(Fwd)
Variant Alleles	A/G
Ancestral Allele	G
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000550844) downstream_gene_variant(ENST00000341259; ENST00000468920; ENST00000550889; ENST00000551551) intron_variant(ENST00000377617; ENST00000389153; ENST00000389154; ENST00000475132; ENST00000483311; ENST00000535949; ENST00000542287; ENST00000550104; ENST00000608853) nc_transcript_variant(ENST00000482777) NMD_transcript_variant(ENST00000483311) non_coding_exon_variant(ENST00000482777) upstream_gene_variant(ENST00000484991)
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: 1)

Genes from other sources (count: 1)

SNPs in LD with rs10849949 (count: 0) View in gBrowse (chr12:111893537..111893537 )