SNP Report

Basic Info

Name	rs11191558 dbSNP Ensembl
Location	chr10:103104921 - 103104921(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.151358
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000343289, ENST00000369857, ENST00000404739, ENST00000452156, ENST00000458345, ENST00000461461, ENST00000470228, ENST00000481549, ENST00000487810, ENST00000552185); NMD_transcript_variant(ENST00000452156, ENST00000461461, ENST00000552185); non_coding_transcript_variant(ENST00000369857, ENST00000470228, ENST00000481549, ENST00000487810)
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 rs11191558 (count: 0) View in gBrowse (chr10:103104921..103104921 )

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

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