SNP Report

Basic Info

Name	rs1049256 dbSNP Ensembl
Location	chr3:49725905 - 49725905(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.401558
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; upstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000321599, ENST00000395238, ENST00000613416); downstream_gene_variant(ENST00000327697, ENST00000433785, ENST00000457726, ENST00000460540, ENST00000468463, ENST00000486102, ENST00000487805, ENST00000495798, ENST00000498376); upstream_gene_variant(ENST00000308375, ENST00000308388, ENST00000480687, ENST00000481959, ENST00000495627)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 3)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
RNF123	ring finger protein 123	3p24.3	Mapped by LD-proxy
GMPPB	GDP-mannose pyrophosphorylase B	3p21.31	Mapped by LD-proxy
IP6K1	inositol hexakisphosphate kinase 1	3p21.31	Mapped by LD-proxy

SNPs in LD with rs1049256 (count: 0) View in gBrowse (chr3:49725905..49725905 )

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

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