SNP Report

Basic Info

Name	rs10865973 dbSNP Ensembl
Location	chr3:52684138 - 52684138(1)
Variant Alleles	A/T
Ancestral Allele	A
Minor Allele	T
Minor Allele Frequence	0.3125
Functional Annotation	intron_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000394830, ENST00000420148, ENST00000424867, ENST00000431678, ENST00000439181, ENST00000449505, ENST00000450271, ENST00000458294, ENST00000479230); upstream_gene_variant(ENST00000296302, ENST00000337303, ENST00000356770, ENST00000394799, ENST00000409057, ENST00000409114, ENST00000409767, ENST00000410007, ENST00000412587, ENST00000418458, ENST00000423351, ENST00000460073, ENST00000462550, ENST00000468146, ENST00000468885, ENST00000474423, ENST00000484022, ENST00000492349, ENST00000496254, ENST00000516978, ENST00000630615)
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)
GNL3	guanine nucleotide binding protein-like 3 (nucleolar)	3p21.1	2(2/0/0)
PBRM1	polybromo 1	3p21	5(4/0/1)

SNPs in LD with rs10865973 (count: 0) View in gBrowse (chr3:52684138..52684138 )

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

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