SNP Report

Basic Info

Name	rs4471726 dbSNP Ensembl
Location	chrCHR_HSCHR17_2_CTG5:45741361 - 45741361(1)
Variant Alleles	T/C
Ancestral Allele	A
Minor Allele	C
Minor Allele Frequence	0.0952476
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000578936, ENST00000580347); intron_variant(ENST00000587305, ENST00000634540); non_coding_transcript_variant(ENST00000587305, ENST00000633260, ENST00000634075, ENST00000631500, ENST00000632599, ENST00000631500, ENST00000632599)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 0)

SNPs in LD with rs4471726 (count: 0) View in gBrowse (chrCHR_HSCHR17_2_CTG5:45741361..45741361 )

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

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