SNP Report

Basic Info
Name rs867198 dbSNP Ensembl
Location chr22:38312601 - 38312601(1)
Variant Alleles C/T
Ancestral Allele C
Minor Allele T
Minor Allele Frequence 0.108227
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000359867, ENST00000396832, ENST00000400206, ENST00000403904, ENST00000405675, ENST00000413574, ENST00000430335)
No. of Studies 0 (Positive: 0; Negative: 0; Trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
CSNK1E casein kinase 1, epsilon 22q13.1 5(1/3/1)

SNPs in LD with rs867198 (count: 0) View in gBrowse (chr22:38312601..38312601 )

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

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