MK4MDD

SNP Report

Basic Information
Name rs3748022 dbSNP Ensembl
Location Chrchr1:206496132(Forward)
Variant Alleles C/T
Ancestral Allele C
Annotation regulatory_region_variant
PolyPhen: 0.021(ENST00000584998, ENST00000581977)
SIFT: tolerated(ENST00000584998, ENST00000581977)
Consequence to Transcript regulatory_region_variant(ENST00000578328, ENST00000584998, ENST00000581977, ENST00000367119)
No. of Studies (Positive/Negative) 1 (0/1) Help

Positive relationship between rs3748022 and MDD (count: 0)
Relationships between rs3748022 and other components at different levels (count: 0) Help
Negative relationships between rs3748022 and MDD (count: 1)
Reference Research Type Statistical Result Relation Description
Traks T, 2015 Patients and nomal controls P-value =0.891 Comparison of allele or haplotype frequencies between cases ...... Comparison of allele or haplotype frequencies between cases and controls was done by chi-squared test. The statistical significance threshold was set to 0.05 for all tests. Ten thousand permutations were used to correct P values for errors of multiple testing. More...

Negative relationships between rs3748022 and other components at different levels (count: 0) Help
rs3748022 related genes (count: 0)