SNP Report

Basic Info

Name	rs6796746 dbSNP Ensembl
Location	chr3:16843728 - 16843728(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.112021
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000460467); non_coding_transcript_variant(ENST00000460467)
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)
PLCL2	phospholipase C-like 2	3p24.3	1(0/1/0)

SNPs in LD with rs6796746 (count: 0) View in gBrowse (chr3:16843728..16843728 )

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

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