SNP Report

Basic Info

Name	rs9890205 dbSNP Ensembl
Location	chr17:30055686 - 30055686(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.441494
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000384284, ENST00000583250, ENST00000584826, ENST00000590718); intron_variant(ENST00000394835, ENST00000419434, ENST00000423598, ENST00000440741, ENST00000536908, ENST00000588978); NMD_transcript_variant(ENST00000423598, ENST00000440741); upstream_gene_variant(ENST00000581617)
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 rs9890205 (count: 0) View in gBrowse (chr17:30055686..30055686 )

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

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