SNP Report

Basic Info

Name	rs2298825 dbSNP Ensembl
Location	chr11:20638137 - 20638137(1)
Variant Alleles	A/C
Ancestral Allele	A
Minor Allele	C
Minor Allele Frequence	0.348243
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000298923, ENST00000525748, ENST00000528440); NMD_transcript_variant(ENST00000298923); non_coding_transcript_variant(ENST00000528440)
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)
SLC6A5	solute carrier family 6 (neurotransmitter transporter), member 5	11p15.1	1(0/1/0)

SNPs in LD with rs2298825 (count: 0) View in gBrowse (chr11:20638137..20638137 )

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

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