SNP Report

Basic Info

Name	rs2236701 dbSNP Ensembl
Location	chr18:13826509 - 13826509(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.264377
Functional Annotation	downstream_gene_variant; synonymous_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000589410); synonymous_variant(ENST00000324750)
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
Lohoff, F. W.,2005(a)	C/T		X² contingency analysis: P-value = 0.581 X² contingency analysis: P-value = 0.581	No significant associations were found in BD. No significant associations were found in BD.	Negative

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
MC5R	melanocortin 5 receptor	18p11.2	1(0/1/0)

SNPs in LD with rs2236701 (count: 0) View in gBrowse (chr18:13826509..13826509 )

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

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