SNP Report

Basic Info

Name	rs12653018 dbSNP Ensembl
Location	chr5:63971009 - 63971009(1)
Variant Alleles	A/C
Ancestral Allele	C
Minor Allele	A
Minor Allele Frequence	0.354433
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000502882); non_coding_transcript_variant(ENST00000502882)
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 rs12653018 (count: 0) View in gBrowse (chr5:63971009..63971009 )

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

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