SNP Report

Basic Info

Name	rs1459549 dbSNP Ensembl
Location	chr4:117686929 - 117686929(1)
Variant Alleles	A/G/T
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.137181
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000422145, ENST00000600624, ENST00000626258, ENST00000630321); non_coding_transcript_variant(ENST00000422145, ENST00000600624, ENST00000626258, ENST00000630321)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 0)

SNPs in LD with rs1459549 (count: 0) View in gBrowse (chr4:117686929..117686929 )

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

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