SNP Report

Basic Info

Name	rs2074613 dbSNP Ensembl
Location	chr5:140334979 - 140334979(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.406749
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000498452); intron_variant(ENST00000230990); non_coding_transcript_exon_variant(ENST00000482211); non_coding_transcript_variant(ENST00000482211)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
HBEGF	heparin-binding EGF-like growth factor	5q23	Mapped by Literature SNP

SNPs in LD with rs2074613 (count: 0) View in gBrowse (chr5:140334979..140334979 )

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

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