SNP Report

Basic Info
Name rs11614604 dbSNP Ensembl
Location chr12:72109907 - 72109907(1)
Variant Alleles C/T
Ancestral Allele C
Minor Allele T
Minor Allele Frequence 0.142772
Functional Annotation intron_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000547278, ENST00000547348, ENST00000548156, ENST00000550403, ENST00000551074); non_coding_transcript_variant(ENST00000547278, ENST00000547348, ENST00000548156, ENST00000550403, ENST00000551074)
No. of Studies 0 (Positive: 0; Negative: 0; Trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
TPH2 tryptophan hydroxylase 2 12q15 13(10/3/0)
TRHDE thyrotropin-releasing hormone degrading enzyme 12q15-q21 Mapped by LD-proxy

SNPs in LD with rs11614604 (count: 0) View in gBrowse (chr12:72109907..72109907 )

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

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