SNP Report

Basic Info
Name rs6031544 dbSNP Ensembl
Location chr20:44353707 - 44353707(1)
Variant Alleles C/T
Ancestral Allele T
Minor Allele T
Minor Allele Frequence 0.35623
Functional Annotation downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000217043); intron_variant(ENST00000438702); non_coding_transcript_variant(ENST00000438702); upstream_gene_variant(ENST00000316673, ENST00000430481, ENST00000457232, ENST00000609262, ENST00000609795, ENST00000619550, LRG_483t1, LRG_483t3)
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)
HNF4A hepatocyte nuclear factor 4, alpha 20q13.12 1(1/0/0)
R3HDML R3H domain containing-like 20q13.12 Mapped by LD-proxy

SNPs in LD with rs6031544 (count: 0) View in gBrowse (chr20:44353707..44353707 )

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

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