SNP Report

Basic Info
Name rs8064449 dbSNP Ensembl
Location chr17:8175711 - 8175711(1)
Variant Alleles G/C
Ancestral Allele G
Minor Allele G
Minor Allele Frequence 0.411941
Functional Annotation intron_variant; non_coding_transcript_variant; stop_gained; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000316425, ENST00000417073, ENST00000431792, ENST00000437139, ENST00000449985, ENST00000526920, ENST00000529756, ENST00000533070); non_coding_transcript_variant(ENST00000417073, ENST00000526920, ENST00000529756); stop_gained(ENST00000532998); upstream_gene_variant(ENST00000363593, ENST00000581248)
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)
TMEM107 transmembrane protein 107 17p13.1 Mapped by LD-proxy
SNORD118 small nucleolar RNA, C/D box 118 17p13.1 Mapped by LD-proxy

SNPs in LD with rs8064449 (count: 0) View in gBrowse (chr17:8175711..8175711 )

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

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