SNP Report

Basic Info

Name	rs3815869 dbSNP Ensembl
Location	chr12:71896820 - 71896820(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.122804
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000468049, ENST00000472611, ENST00000474468, ENST00000482439, ENST00000549402); intron_variant(ENST00000319106, ENST00000462788, ENST00000483828, ENST00000485960, ENST00000491063, ENST00000550746); NMD_transcript_variant(ENST00000462788); non_coding_transcript_variant(ENST00000483828); upstream_gene_variant(ENST00000479971, ENST00000548679)
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)
TBC1D15	TBC1 domain family, member 15	12q15	Mapped by Literature SNP

SNPs in LD with rs3815869 (count: 0) View in gBrowse (chr12:71896820..71896820 )

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

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