SNP Report

Basic Info

Name	rs4077465 dbSNP Ensembl
Location	chr17:29973126 - 29973126(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.457668
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000421238, ENST00000448319, ENST00000581995); intron_variant(ENST00000394835, ENST00000419434, ENST00000423598, ENST00000440741, ENST00000534836, ENST00000536908, ENST00000588978); NMD_transcript_variant(ENST00000423598, ENST00000440741); non_coding_transcript_variant(ENST00000534836)
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)
EFCAB5	EF-hand calcium binding domain 5	17q11.2	Mapped by Literature SNP

SNPs in LD with rs4077465 (count: 0) View in gBrowse (chr17:29973126..29973126 )

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

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