SNP Report

Basic Info

Name	rs11079717 dbSNP Ensembl
Location	chrCHR_HSCHR17_2_CTG5:45769580 - 45769580(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.0894569
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000587305, ENST00000634540); non_coding_transcript_variant(ENST00000587305, ENST00000631500, ENST00000632599, ENST00000631500, ENST00000632599)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 0)

SNPs in LD with rs11079717 (count: 0) View in gBrowse (chrCHR_HSCHR17_2_CTG5:45769580..45769580 )

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

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