SNP Report

Basic Info

Name	rs2164885 dbSNP Ensembl
Location	chr3:52697253 - 52697253(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.445487
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000391150, ENST00000394799, ENST00000418458, ENST00000464705, ENST00000484022, ENST00000487642, ENST00000496254, ENST00000497356, ENST00000497436, ENST00000497953); intron_variant(ENST00000266014, ENST00000394783, ENST00000463827, ENST00000478968, ENST00000479553, ENST00000484163, ENST00000485899, ENST00000489119, ENST00000491606); non_coding_transcript_variant(ENST00000463827, ENST00000484163, ENST00000485899); upstream_gene_variant(ENST00000480080, ENST00000481643)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 3)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
GLT8D1	glycosyltransferase 8 domain containing 1	3p21.1	1(1/0/0)
SNORD69	small nucleolar RNA, C/D box 69	3p21.1	Mapped by Literature SNP
GNL3	guanine nucleotide binding protein-like 3 (nucleolar)	3p21.1	2(2/0/0)

SNPs in LD with rs2164885 (count: 0) View in gBrowse (chr3:52697253..52697253 )

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

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