SNP Report

Basic Info

Name	rs12469225 dbSNP Ensembl
Location	chr2:11901816 - 11901816(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.36881
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000438292); non_coding_transcript_variant(ENST00000438292)
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 rs12469225 (count: 0) View in gBrowse (chr2:11901816..11901816 )

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

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