SNP Report

Basic Info

Name	rs4760822 dbSNP Ensembl
Location	chr12:72085831 - 72085831(1)
Variant Alleles	T/G
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.213059
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000547278, ENST00000547348, ENST00000550403, ENST00000551074); non_coding_transcript_variant(ENST00000547278, ENST00000547348, ENST00000550403, ENST00000551074); upstream_gene_variant(ENST00000548156)
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 rs4760822 (count: 0) View in gBrowse (chr12:72085831..72085831 )

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

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