SNP Report

Basic Info

Name	rs1467048 dbSNP Ensembl
Location	chr8:130012301 - 130012301(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.199281
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000401979, ENST00000517654, ENST00000518167, ENST00000518283, ENST00000518285, ENST00000518879, ENST00000519020, ENST00000519110, ENST00000521223, ENST00000522361, ENST00000522702, ENST00000523288, ENST00000523509, ENST00000523514, ENST00000523993); non_coding_transcript_variant(ENST00000518285, ENST00000518879, ENST00000521223, ENST00000522702, ENST00000523288, ENST00000523514); upstream_gene_variant(ENST00000582634)
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)
FAM49B	family with sequence similarity 49, member B	8q24.21	1(0/1/0)
MIR5194	microRNA 5194	8	Mapped by LD-proxy

SNPs in LD with rs1467048 (count: 0) View in gBrowse (chr8:130012301..130012301 )

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

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