SNP Report

Basic Info
Name rs1775715 dbSNP Ensembl
Location chr10:32020077 - 32020077(1)
Variant Alleles A/G
Ancestral Allele A
Minor Allele G
Minor Allele Frequence 0.485423
Functional Annotation intron_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000302418, ENST00000493889); non_coding_transcript_variant(ENST00000493889)
No. of Studies 1 (Positive: 0; Negative: 0; Trend: 1)
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
Goes, F. S.,2012 G OR = 1.18,P-value(Meta) = 0.00000513 OR = 1.18,P-value(Meta) = 0.00000513 Suggestive association was found. Suggestive association was found. Trend

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
KIF5B kinesin family member 5B 10p11.22 1(0/0/1)

SNPs in LD with rs1775715 (count: 66) View in gBrowse (chr10:31821979..32050864 )
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.

Literature-origin SNPs (count: 0)

LD-proxies (count: 66)

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

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