SNP Report

Basic Info

Name	rs1075653 dbSNP Ensembl
Location	chr3:52791512 - 52791512(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.398762
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; splice_region_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000482836, ENST00000484844); intron_variant(ENST00000273283, ENST00000405128, ENST00000428133, ENST00000494705, ENST00000537050, ENST00000628722); non_coding_transcript_variant(ENST00000494705, ENST00000628722); splice_region_variant(ENST00000273283, ENST00000405128, ENST00000428133, ENST00000494705, ENST00000537050, ENST00000628722); upstream_gene_variant(ENST00000416872, ENST00000449956, ENST00000467268, ENST00000621946)
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)
ITIH3	inter-alpha-trypsin inhibitor heavy chain 3	3p21.1	3(3/0/0)
ITIH1	inter-alpha-trypsin inhibitor heavy chain 1	3p21.1	1(1/0/0)

SNPs in LD with rs1075653 (count: 0) View in gBrowse (chr3:52791512..52791512 )

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

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