SNP Report

Basic Info

Name	rs2696588 dbSNP Ensembl
Location	chrCHR_HSCHR17_2_CTG5:46156661 - 46156661(1)
Variant Alleles	G/C
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.422125
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000262419, ENST00000432791, ENST00000572904, ENST00000574590, ENST00000575318, ENST00000577114); non_coding_transcript_variant(ENST00000577114, ENST00000611596, ENST00000626533, ENST00000627698, ENST00000629551, ENST00000630200, ENST00000630234, ENST00000630234, ENST00000610328, ENST00000613150, ENST00000622036, ENST00000633346, ENST00000633521, ENST00000633819, ENST00000633521)
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)
KANSL1	KAT8 regulatory NSL complex subunit 1	17q21.31	Mapped by Literature SNP

SNPs in LD with rs2696588 (count: 0) View in gBrowse (chrCHR_HSCHR17_2_CTG5:46156661..46156661 )

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

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