SNP Report

Basic Info
Name rs2887147 dbSNP Ensembl
Location chr12:71994480 - 71994480(1)
Variant Alleles C/A/T
Ancestral Allele C
Minor Allele Frequence 0.0
Functional Annotation missense_variant.
Polyphen Annotation: possibly damaging(ENST00000333850' target='_blank'>ENST00000333850); probably damaging(ENST00000333850' target='_blank'>ENST00000333850)
SIFT Annotation: deleterious(ENST00000333850)
Consequence to Transcript missense_variant(ENST00000333850, ENST00000333850)
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)
TPH2 tryptophan hydroxylase 2 12q15 13(10/3/0)

SNPs in LD with rs2887147 (count: 0) View in gBrowse (chr12:71994480..71994480 )

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

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