SNP Report

Basic Info

Name	rs3858589 dbSNP Ensembl
Location	chr12:72105543 - 72105543(1)
Variant Alleles	A/C
Ancestral Allele	C
Minor Allele	A
Minor Allele Frequence	0.204073
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 rs3858589 (count: 0) View in gBrowse (chr12:72105543..72105543 )

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

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