SNP Report

Basic Info

Name	rs116719 dbSNP Ensembl
Location	chr17:76754249 - 76754249(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.11262
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000363387); intron_variant(ENST00000336509, ENST00000355954, ENST00000585584, ENST00000585958, ENST00000586622, ENST00000588460, ENST00000588670, ENST00000588768, ENST00000590514, ENST00000593181, ENST00000621483); NMD_transcript_variant(ENST00000585584, ENST00000588670, ENST00000588768); non_coding_transcript_variant(ENST00000585958)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
MFSD11	major facilitator superfamily domain containing 11	17q25.1	1(0/1/0)
RNU6-97P	RNA, U6 small nuclear 97, pseudogene	17q25.1	Mapped by LD-proxy

SNPs in LD with rs116719 (count: 0) View in gBrowse (chr17:76754249..76754249 )

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

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