SNP Report

Basic Info
| Name |
rs7545321
dbSNP
Ensembl
|
| Location |
chr1:31656563 - 31656563(1) |
| Variant Alleles |
A/G |
| Ancestral Allele |
G |
| Minor Allele |
A |
| Minor Allele Frequence |
0.466054 |
| Functional Annotation |
downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
|
| Consequence to Transcript |
downstream_gene_variant(ENST00000466829, ENST00000470799, ENST00000482910); intron_variant(ENST00000373672, ENST00000440437, ENST00000445166, ENST00000488128, ENST00000488897, ENST00000585413, ENST00000585660, ENST00000587445, ENST00000589462, ENST00000591592, ENST00000591929, ENST00000593188, ENST00000607926, ENST00000608246, ENST00000608332, ENST00000608888, ENST00000609033, ENST00000609338, ENST00000609373, ENST00000609549, ENST00000609625, ENST00000610043, ENST00000610216, ENST00000623425, ENST00000623786, ENST00000623791, ENST00000624388); non_coding_transcript_variant(ENST00000445166, ENST00000488128, ENST00000488897, ENST00000585413, ENST00000585660, ENST00000587445, ENST00000589462, ENST00000591592, ENST00000591929, ENST00000593188, ENST00000607926, ENST00000608246, ENST00000608332, ENST00000608888, ENST00000609033, ENST00000609338, ENST00000609373, ENST00000609549, ENST00000609625, ENST00000610043, ENST00000610216, ENST00000623425, ENST00000623786, ENST00000623791, ENST00000624388); upstream_gene_variant(ENST00000461217, ENST00000588288) |
| No. of Studies |
0 (Positive: 0; Negative: 0; Trend: 0) |
| Source |
LD-proxy |

SNP related studies (count: 0)

SNP related genes (count: 1)

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

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