SNP Report

Basic Info

Name	rs685657 dbSNP Ensembl
Location	chr11:18039122 - 18039122(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.305112
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000250018, ENST00000417164, ENST00000528338); NMD_transcript_variant(ENST00000417164)
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)
TPH1	tryptophan hydroxylase 1	11p15.3-p14	14(5/9/0)

SNPs in LD with rs685657 (count: 0) View in gBrowse (chr11:18039122..18039122 )

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

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