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)