SNP Report

Basic Info
Name rs6787318 dbSNP Ensembl
Location chr3:197742767 - 197742767(1)
Variant Alleles C/T
Ancestral Allele C
Minor Allele C
Minor Allele Frequence 0.261382
Functional Annotation intron_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000273582, ENST00000428738, ENST00000467303); non_coding_transcript_variant(ENST00000467303)
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)
FYTTD1 forty-two-three domain containing 1 3q29 1(0/1/0)
KIAA0226 KIAA0226 3q29 Mapped by Literature SNP

SNPs in LD with rs6787318 (count: 0) View in gBrowse (chr3:197742767..197742767 )

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

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