SNP Report

Basic Info

Name	rs11594610 dbSNP Ensembl
Location	chr10:113153224 - 113153224(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.104832
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000369389, ENST00000636236, ENST00000636309, ENST00000636447, ENST00000637321, ENST00000637416); intron_variant(ENST00000277945, ENST00000352065, ENST00000355717, ENST00000355995, ENST00000369386, ENST00000369395, ENST00000369397, ENST00000466338, ENST00000470254, ENST00000480888, ENST00000534894, ENST00000536810, ENST00000538897, ENST00000542695, ENST00000543371, ENST00000545257, ENST00000627217, ENST00000629706); NMD_transcript_variant(ENST00000470254); upstream_gene_variant(ENST00000471569)
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)
TCF7L2	transcription factor 7-like 2 (T-cell specific, HMG-box)	10q25.3	1(1/0/0)

SNPs in LD with rs11594610 (count: 0) View in gBrowse (chr10:113153224..113153224 )

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

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