SNP Report

Basic Info

Name	rs11191555 dbSNP Ensembl
Location	chr10:103097766 - 103097766(1)
Variant Alleles	A/C
Ancestral Allele	A
Minor Allele	C
Minor Allele Frequence	0.151558
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000458345, ENST00000470228, ENST00000481549, ENST00000487810, ENST00000552185); intron_variant(ENST00000343289, ENST00000369857, ENST00000404739, ENST00000452156, ENST00000461461); NMD_transcript_variant(ENST00000452156, ENST00000461461); non_coding_transcript_variant(ENST00000369857); upstream_gene_variant(ENST00000421281, ENST00000469228)
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)
NT5C2	5'-nucleotidase, cytosolic II	10q24.32	2(2/0/0)

SNPs in LD with rs11191555 (count: 0) View in gBrowse (chr10:103097766..103097766 )

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

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