SNP Report

Basic Info

Name	rs2292165 dbSNP Ensembl
Location	chr1:31260045 - 31260045(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.224241
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000263694, ENST00000373720); downstream_gene_variant(ENST00000452686); non_coding_transcript_exon_variant(ENST00000486941, ENST00000489853, ENST00000491106); non_coding_transcript_variant(ENST00000486941, ENST00000489853, ENST00000491106)
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)
SNRNP40	small nuclear ribonucleoprotein 40kDa (U5)	1p35.2	Mapped by LD-proxy

SNPs in LD with rs2292165 (count: 0) View in gBrowse (chr1:31260045..31260045 )

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

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