SNP Report

Basic Info

Name	rs174601 dbSNP Ensembl
Location	chr11:61855668 - 61855668(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.492412
Functional Annotation	intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000257261, ENST00000278840, ENST00000355484, ENST00000521571, ENST00000521849, ENST00000522056); non_coding_transcript_exon_variant(ENST00000523235); non_coding_transcript_variant(ENST00000523235)
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)
FADS2	fatty acid desaturase 2	11q12.2	Mapped by Literature SNP

SNPs in LD with rs174601 (count: 0) View in gBrowse (chr11:61855668..61855668 )

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

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