SNP Report

Basic Info

Name	rs407692 dbSNP Ensembl
Location	chr12:119789119 - 119789119(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.442093
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000261833, ENST00000392520, ENST00000392521, ENST00000488203, ENST00000536325, ENST00000539413, ENST00000545913, ENST00000612548); non_coding_transcript_variant(ENST00000488203, ENST00000539413, ENST00000545913); upstream_gene_variant(ENST00000537607)
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)
CIT	citron rho-interacting serine/threonine kinase	12q24.23	2(1/1/0)

SNPs in LD with rs407692 (count: 0) View in gBrowse (chr12:119789119..119789119 )

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

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