SNP Report

Basic Info

Name	rs1805474 dbSNP Ensembl
Location	chr12:13589216 - 13589216(1)
Variant Alleles	T/G
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.290335
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 rs1805474 (count: 0) View in gBrowse (chr12:13589216..13589216 )

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

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