SNP Report

Basic Info

Name	rs3136055 dbSNP Ensembl
Location	chr16:13921720 - 13921720(1)
Variant Alleles	C/G
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.0325479
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000463867); intron_variant(ENST00000311895, ENST00000575156, ENST00000576348, LRG_463t1); non_coding_transcript_variant(ENST00000576348); upstream_gene_variant(ENST00000574194)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
ERCC4	excision repair cross-complementation group 4	16p13.3	1(0/0/1)
RPS26P52	ribosomal protein S26 pseudogene 52	16p13.3	Mapped by LD-proxy

SNPs in LD with rs3136055 (count: 0) View in gBrowse (chr16:13921720..13921720 )

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

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