SNP Report

Basic Info
Name |
rs2279020
dbSNP
Ensembl
|
Location |
chr5:161895883 - 161895883(1) |
Variant Alleles |
G/A |
Ancestral Allele |
A |
Minor Allele |
G |
Minor Allele Frequence |
0.403954 |
Functional Annotation |
downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
|
Consequence to Transcript |
downstream_gene_variant(ENST00000519542, ENST00000634335); intron_variant(ENST00000023897, ENST00000393943, ENST00000428797, ENST00000437025, ENST00000635880, ENST00000636340, ENST00000636408, ENST00000636573, ENST00000637044, ENST00000637827, ENST00000638112, ENST00000638159); NMD_transcript_variant(ENST00000636340, ENST00000637044); non_coding_transcript_variant(ENST00000636408) |
No. of Studies |
1 (Positive: 0; Negative: 1; Trend: 0) |
Source |
Literature |
Overlap with SZ? |
NO
|
Overlap with MDD? |
YES
|

SNP related studies (count: 1)

SNP related genes (count: 1)

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

Overlap with MDD from cross-disorder studies (count: 1)
Reference |
Statistical Result |
Description |
Result Category |
Horiuchi, Y.,2004 |
Association analysis:genotype P-value = 0.55, allele P-value = 0.58 |
No significant association was observed. |
Negative
|