SNP Report

Basic Info
Name rs971846 dbSNP Ensembl
Location chr7:103491048 - 103491048(1)
Variant Alleles A/C
Ancestral Allele A
Minor Allele C
Minor Allele Frequence 0.234425
Functional Annotation intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000343529, ENST00000422488, ENST00000424685, ENST00000428762); non_coding_transcript_variant(ENST00000422488); upstream_gene_variant(ENST00000473945)
No. of Studies 0 (Positive: 0; Negative: 0; Trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
RELN reelin 7q22 3(1/2/0)

SNPs in LD with rs971846 (count: 0) View in gBrowse (chr7:103491048..103491048 )

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

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