SNP Report

Basic Info

Name	rs174568 dbSNP Ensembl
Location	chr11:61826344 - 61826344(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.296126
Functional Annotation	3_prime_UTR_variant; intron_variant; synonymous_variant; upstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000517839); intron_variant(ENST00000257261, ENST00000421879, ENST00000448607, ENST00000522056); synonymous_variant(ENST00000522639, ENST00000574708); upstream_gene_variant(ENST00000278840, ENST00000517312, ENST00000518606, ENST00000521849)
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)
FADS2	fatty acid desaturase 2	11q12.2	Mapped by Literature SNP
FADS1	fatty acid desaturase 1	11q12-q13.1	Mapped by LD-proxy

SNPs in LD with rs174568 (count: 0) View in gBrowse (chr11:61826344..61826344 )

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

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