SNP Report

Basic Info

Name	rs3801727 dbSNP Ensembl
Location	chr7:82162685 - 82162685(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.125599
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000356253, ENST00000356860, ENST00000423588, ENST00000484706, LRG_437t1); non_coding_transcript_variant(ENST00000484706)
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)
CACNA2D1	calcium channel, voltage-dependent, alpha 2/delta subunit 1	7q21-q22	2(0/0/2)

SNPs in LD with rs3801727 (count: 0) View in gBrowse (chr7:82162685..82162685 )

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

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