SNP Report

Basic Info

Name	rs2071044 dbSNP Ensembl
Location	chr3:52813585 - 52813585(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.447284
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000416872, ENST00000449956, ENST00000461966, ENST00000481977, ENST00000493136, ENST00000537897, ENST00000621946); intron_variant(ENST00000266041, ENST00000406595, ENST00000441637, ENST00000464000, ENST00000468472, ENST00000485816, ENST00000491663); NMD_transcript_variant(ENST00000468472); non_coding_transcript_variant(ENST00000464000, ENST00000491663)
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)
ITIH3	inter-alpha-trypsin inhibitor heavy chain 3	3p21.1	3(3/0/0)
ITIH4	inter-alpha-trypsin inhibitor heavy chain family, member 4	3p21.1	Mapped by Literature SNP
MUSTN1	musculoskeletal, embryonic nuclear protein 1	3p21.31	Mapped by Literature SNP

SNPs in LD with rs2071044 (count: 0) View in gBrowse (chr3:52813585..52813585 )

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

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