SNP Report

Basic Info
| Name |
rs1079598
dbSNP
Ensembl
|
| Location |
11:113425552 - 113425552(+) |
| Variant Seq |
G |
| Ancestral Allele |
A |
| Ref Seq |
A |
| Minor Allele Frequence |
0.227835 |
| Annotation |
upstream_gene_variant; intron_variant; non_coding_transcript_variant
|
| Variant Effect |
upstream_gene_variant(ENST00000542968, ENST00000544518, ENST00000535984, ENST00000538967); intron_variant(ENST00000346454, ENST00000540600, ENST00000543292, ENST00000362072, ENST00000542616); non_coding_transcript_variant(ENST00000540600)
|
| SIFT Annotation |
tolerated_-_low_confidence; tolerated
|
| SIFT Variant Effect |
tolerated_-_low_confidence(ENST00000362072, ENST00000542968, ENST00000544518); tolerated(ENST00000346454, ENST00000543292, ENST00000538967)
|
| PolyPhen Annotation |
benign
|
| PolyPhen Variant Effect |
benign(ENST00000362072, ENST00000346454, ENST00000543292, ENST00000542968, ENST00000544518, ENST00000538967)
|
| rSNP? |
Yes
Link in rVarBase
|
| Related Regulatory Elements |
n/a
|
| 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: 1)

SNPs in LD with rs1079598 (count: 0)

SNP related eQTL (count: 1)