SNP Report

Basic Info

Name	rs4074170 dbSNP Ensembl
Location	chr17:30054123 - 30054123(1)
Variant Alleles	C/G
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.429113
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; NMD_transcript_variant; synonymous_variant; upstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000423598); downstream_gene_variant(ENST00000384284, ENST00000584826, ENST00000590718); NMD_transcript_variant(ENST00000423598, ENST00000440741); synonymous_variant(ENST00000394835, ENST00000419434, ENST00000440741, ENST00000536908, ENST00000588978); 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 rs4074170 (count: 0) View in gBrowse (chr17:30054123..30054123 )

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

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