SNP Report

Basic Info

Name	rs266156 dbSNP Ensembl
Location	chr2:107493669 - 107493669(1)
Variant Alleles	T/G
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.300719
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000414300); non_coding_transcript_variant(ENST00000414300)
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 rs266156 (count: 0) View in gBrowse (chr2:107493669..107493669 )

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

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