SNP Report

Basic Info

Name	rs12521757 dbSNP Ensembl
Location	chr5:151214634 - 151214634(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.26897
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000519740); intron_variant(ENST00000355417, ENST00000521308, ENST00000523466); non_coding_transcript_variant(ENST00000521308); upstream_gene_variant(ENST00000522179)
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)
CCDC69	coiled-coil domain containing 69	5q33.1	1(1/0/0)
GM2A	GM2 ganglioside activator	5q33.1	Mapped by Literature SNP

SNPs in LD with rs12521757 (count: 0) View in gBrowse (chr5:151214634..151214634 )

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

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