SNP Report

Basic Info

Name	rs9890886 dbSNP Ensembl
Location	chr17:30064058 - 30064058(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.440296
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000581617); intron_variant(ENST00000394835, ENST00000419434, ENST00000423598, ENST00000440741, ENST00000536908, ENST00000583250, ENST00000588978); NMD_transcript_variant(ENST00000423598, ENST00000440741); non_coding_transcript_variant(ENST00000583250); upstream_gene_variant(ENST00000384284, ENST00000583091, ENST00000590718)
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)
EFCAB5	EF-hand calcium binding domain 5	17q11.2	Mapped by Literature SNP
RNY4P13	RNA, Ro-associated Y4 pseudogene 13	17q11.2	Mapped by Literature SNP

SNPs in LD with rs9890886 (count: 0) View in gBrowse (chr17:30064058..30064058 )

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

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