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)