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)