SNP Report

Basic Info

Name	rs12316898 dbSNP Ensembl
Location	chr12:102264195 - 102264195(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.0656949
Functional Annotation	non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	non_coding_transcript_exon_variant(ENST00000626826); non_coding_transcript_variant(ENST00000626826)
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 rs12316898 (count: 0) View in gBrowse (chr12:102264195..102264195 )

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

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