SNP Report

Basic Info

Name	rs1165666 dbSNP Ensembl
Location	chr12:103923758 - 103923758(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.226837
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000388789, ENST00000548897); non_coding_transcript_variant(ENST00000388789, ENST00000548897)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 0)

SNPs in LD with rs1165666 (count: 0) View in gBrowse (chr12:103923758..103923758 )

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

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