SNP Report

Basic Info
| Name |
rs2456019
dbSNP
Ensembl
|
| Location |
15:78576147 - 78576147(+) |
| Variant Seq |
G |
| Ancestral Allele |
G |
| Ref Seq |
T |
| Minor Allele Frequence |
0.239816 |
| Annotation |
upstream_gene_variant; intron_variant
|
| Variant Effect |
upstream_gene_variant(ENST00000394802); intron_variant(ENST00000299565, ENST00000559554)
|
| SIFT Annotation |
tolerated
|
| SIFT Variant Effect |
tolerated(ENST00000044462, ENST00000413382, ENST00000559154, ENST00000559948, ENST00000559365, ENST00000560217, ENST00000559082, ENST00000560737, ENST00000558094, ENST00000558281, ENST00000559437, ENST00000559146)
|
| PolyPhen Annotation |
benign
|
| PolyPhen Variant Effect |
benign(ENST00000044462, ENST00000413382, ENST00000559154, ENST00000559948, ENST00000559365, ENST00000560217, ENST00000559082, ENST00000560737, ENST00000558094, ENST00000558281, ENST00000559437, ENST00000559146)
|
| rSNP? |
Yes
Link in rVarBase
|
| Related Regulatory Elements |
Chromatin interactive region
|
| Chromatin State |
Weak transcription
|
| No. of Marker's Association Results |
0 (Positive: 0; Negative: 0; Trend: 0) |
| Source |
LD-proxy |

SNP related association results

SNP related genes (count: 2)

SNPs in LD with rs2456019 (count: 0)

SNP related eQTL (count: 1)