SNP Report

Basic Info
Name rs13030726 dbSNP Ensembl
Location chr2:115492547 - 115492547(1)
Variant Alleles C/T
Ancestral Allele C
Minor Allele T
Minor Allele Frequence 0.304513
Functional Annotation intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000310323, ENST00000393146, ENST00000393147, ENST00000409163, ENST00000410059, ENST00000419287, ENST00000429914, ENST00000436732, ENST00000461250, ENST00000486885, ENST00000488208); NMD_transcript_variant(ENST00000429914); non_coding_transcript_variant(ENST00000461250, ENST00000486885, ENST00000488208)
No. of Studies 0 (Positive: 0; Negative: 0; Trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
DPP10 dipeptidyl-peptidase 10 (non-functional) 2q14.1 3(2/1/0)

SNPs in LD with rs13030726 (count: 0) View in gBrowse (chr2:115492547..115492547 )

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)