SNP Report

Basic Info

Name	rs1806199 dbSNP Ensembl
Location	chr12:13582220 - 13582220(1)
Variant Alleles	A/T
Ancestral Allele	A
Minor Allele	T
Minor Allele Frequence	0.0920527
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000609686, ENST00000628166, ENST00000637214); non_coding_transcript_variant(ENST00000628166)
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 rs1806199 (count: 0) View in gBrowse (chr12:13582220..13582220 )

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

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