SNP Report

Basic Info
Name rs7331595 dbSNP Ensembl
Location chr13:98945478 - 98945478(1)
Variant Alleles C/A
Ancestral Allele A
Minor Allele A
Minor Allele Frequence 0.465056
Functional Annotation downstream_gene_variant; intron_variant; NMD_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000417594); intron_variant(ENST00000339416, ENST00000376460, ENST00000427887, ENST00000442173, ENST00000448493, ENST00000627024, ENST00000630992); NMD_transcript_variant(ENST00000339416, ENST00000630992)
No. of Studies 1 (Positive: 0; Negative: 1; Trend: 0)
Source Literature
Overlap with SZ? NO
Overlap with MDD? NO

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result Category
Detera-Wadleigh, S. D., 2007 FBAT-e P-value = 0.435 in NIMH1-2 FBAT-e P-value = 0.435 in NIMH1-2 no significant over-transmission of any alleles was detected no significant over-transmission of any alleles was detected Negative

SNP related genes (count: 2)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
RPL7L1P12 ribosomal protein L7-like 1 pseudogene 12 13q32.3 Mapped by Literature SNP
DOCK9 dedicator of cytokinesis 9 13q32.3 1(1/0/0)

SNPs in LD with rs7331595 (count: 0) View in gBrowse (chr13:98945478..98945478 )

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

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