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)