SNP Report

Basic Info

Name	rs5750581 dbSNP Ensembl
Location	chr22:38299401 - 38299401(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.118211
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000430335); intron_variant(ENST00000359867, ENST00000396832, ENST00000400206, ENST00000403904, ENST00000405675, ENST00000413574, ENST00000431611, ENST00000442216, ENST00000451964, ENST00000498529, ENST00000612795); NMD_transcript_variant(ENST00000431611, ENST00000442216); non_coding_transcript_variant(ENST00000498529, ENST00000612795); upstream_gene_variant(ENST00000366216, ENST00000431632, ENST00000494610, ENST00000495232)
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 rs5750581 (count: 0) View in gBrowse (chr22:38299401..38299401 )

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

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