SNP Report

Basic Info

Name	rs174555 dbSNP Ensembl
Location	chr11:61812288 - 61812288(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.279553
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000410394, ENST00000448607, ENST00000473263, ENST00000539419, ENST00000541683, ENST00000545986); intron_variant(ENST00000350997, ENST00000421879, ENST00000424501, ENST00000433932, ENST00000466716, ENST00000491310, ENST00000496123, ENST00000540767, ENST00000542506, ENST00000544309, ENST00000544696, ENST00000545245, ENST00000545405, ENST00000574708); NMD_transcript_variant(ENST00000424501); non_coding_transcript_variant(ENST00000496123); upstream_gene_variant(ENST00000257261, ENST00000517839, ENST00000522056, ENST00000522639, ENST00000539999)
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 rs174555 (count: 0) View in gBrowse (chr11:61812288..61812288 )

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

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