SNP Report

Basic Info

Name	rs739496 dbSNP Ensembl
Location	chr12:111449855 - 111449855(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.415136
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000341259, LRG_621t1, LRG_621t2); downstream_gene_variant(ENST00000377617, ENST00000389153, ENST00000389154, ENST00000475132, ENST00000482777, ENST00000483311, ENST00000484991, ENST00000535949, ENST00000538307, ENST00000542287, ENST00000550104, ENST00000550844, ENST00000608853, ENST00000616825)
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)
SH2B3	SH2B adaptor protein 3	12q24.12	Mapped by Literature SNP
ATXN2	ataxin 2	12q23-q24.1	Mapped by LD-proxy

SNPs in LD with rs739496 (count: 0) View in gBrowse (chr12:111449855..111449855 )

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

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