SNP Report

Basic Info

Name	rs2139569 dbSNP Ensembl
Location	chr12:102370626 - 102370626(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.470248
Functional Annotation	intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000635615); non_coding_transcript_exon_variant(ENST00000626826); non_coding_transcript_variant(ENST00000626826, ENST00000635615)
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 rs2139569 (count: 0) View in gBrowse (chr12:102370626..102370626 )

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

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