SNP Report

Basic Info

Name	rs38452 dbSNP Ensembl
Location	chr7:30534036 - 30534036(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.268371
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000583191); intron_variant(ENST00000434399, ENST00000578293, ENST00000580902, ENST00000598361, ENST00000626902, ENST00000631229); non_coding_transcript_variant(ENST00000434399, ENST00000578293, ENST00000580902, ENST00000626902, ENST00000631229)
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 rs38452 (count: 0) View in gBrowse (chr7:30534036..30534036 )

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

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