SNP Report

Basic Info
| Name |
rs1615409
dbSNP
Ensembl
|
| Location |
chr1:231547671 - 231547671(1) |
| Variant Alleles |
C/A |
| Ancestral Allele |
A |
| Minor Allele |
C |
| Minor Allele Frequence |
0.460264 |
| Functional Annotation |
downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
|
| Consequence to Transcript |
downstream_gene_variant(ENST00000476913); intron_variant(ENST00000366639, ENST00000413309, ENST00000475168, ENST00000602567, ENST00000602634, ENST00000602825, ENST00000602885, ENST00000602956, ENST00000602962); NMD_transcript_variant(ENST00000602567, ENST00000602634, ENST00000602885, ENST00000602956, ENST00000602962); non_coding_transcript_variant(ENST00000475168, ENST00000602825) |
| No. of Studies |
2 (Positive: 0; Negative: 2; Trend: 0) |
| Source |
Literature |
| Overlap with SZ? |
YES
|
| Overlap with MDD? |
NO
|

SNP related studies (count: 2)

SNP related genes (count: 2)

Overlap with SZ from cross-disorder studies (count: 1)
| Reference |
Statistical Result |
Description |
Result Category |
| Thomson, P. A.,2005(a) |
Single-Marker Analysis:allele frequency, for SZ, P-value = 0.86 |
No significant association was observed. |
Negative |

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