SNP Report

Basic Info
| Name |
rs1362620
dbSNP
Ensembl
|
| Location |
16:55654462 - 55654462(+) |
| Variant Seq |
C |
| Ancestral Allele |
C |
| Ref Seq |
T |
| Minor Allele Frequence |
0.236222 |
| Annotation |
upstream_gene_variant
|
| Variant Effect |
upstream_gene_variant(ENST00000568655, ENST00000379906, ENST00000561820, ENST00000566163, ENST00000568943, ENST00000568529, ENST00000219833, ENST00000414754)
|
| SIFT Annotation |
deleterious
|
| SIFT Variant Effect |
deleterious(ENST00000568529, ENST00000379906, ENST00000566163, ENST00000219833, ENST00000414754, ENST00000561820, ENST00000568655, ENST00000568943)
|
| PolyPhen Annotation |
benign; possibly_damaging; probably_damaging
|
| PolyPhen Variant Effect |
benign(ENST00000414754); possibly_damaging(ENST00000561820); probably_damaging(ENST00000568529, ENST00000379906, ENST00000566163, ENST00000219833, ENST00000568655, ENST00000568943)
|
| rSNP? |
Yes
Link in rVarBase
|
| Related Regulatory Elements |
TF binding region
|
| Chromatin State |
Bivalent Enhancer
|
| 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 rs1362620 (count: 0)

SNP related eQTL (count: 1)