SNP Report

Basic Info
| Name |
rs16854809
dbSNP
Ensembl
|
| Location |
chr1:231703501 - 231703501(1) |
| Variant Alleles |
A/G |
| Ancestral Allele |
G |
| Minor Allele |
G |
| Minor Allele Frequence |
0.300519 |
| Functional Annotation |
downstream_gene_variant; intron_variant; NMD_transcript_variant.
|
| Consequence to Transcript |
downstream_gene_variant(ENST00000468399); intron_variant(ENST00000295051, ENST00000317586, ENST00000366632, ENST00000366633, ENST00000366636, ENST00000366637, ENST00000422590, ENST00000439617, ENST00000535944, ENST00000535983, ENST00000537876, ENST00000539444, ENST00000602281, ENST00000602567, ENST00000602634, ENST00000602700, ENST00000602713, ENST00000602822, ENST00000602873, ENST00000602885, ENST00000602956, ENST00000602962, ENST00000620189, ENST00000622252, ENST00000628350); NMD_transcript_variant(ENST00000295051, ENST00000366632, ENST00000422590, ENST00000535944, ENST00000602567, ENST00000602634, ENST00000602700, ENST00000602713, ENST00000602822, ENST00000602885, ENST00000602956, ENST00000602962) |
| 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)