SNP Report

Basic Info
Name |
rs10482605
dbSNP
Ensembl
|
Location |
5:143403956 - 143403956(+) |
Variant Seq |
G |
Ancestral Allele |
A |
Ref Seq |
A |
Minor Allele Frequence |
0.0982428 |
Annotation |
upstream_gene_variant; intron_variant
|
Variant Effect |
upstream_gene_variant(ENST00000415690, ENST00000510170, ENST00000424646, ENST00000231509, ENST00000502500, ENST00000394464, ENST00000508760, ENST00000623204); intron_variant(ENST00000503201, ENST00000343796, ENST00000502892, ENST00000514699, ENST00000504572, ENST00000394466)
|
SIFT Annotation |
tolerated
|
SIFT Variant Effect |
tolerated(ENST00000424646, ENST00000504572, ENST00000503201, ENST00000231509, ENST00000394466, ENST00000343796, ENST00000394464, ENST00000415690)
|
PolyPhen Annotation |
benign
|
PolyPhen Variant Effect |
benign(ENST00000424646, ENST00000504572, ENST00000503201, ENST00000231509, ENST00000394466, ENST00000343796, ENST00000394464, ENST00000415690)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
TF binding region;Chromatin interactive region
|
Chromatin State |
Active TSS;Bivalent/Poised TSS;Transcr. at gene 5' nd 3';Weak transcription
|
No. of Marker's Association Results |
1 (Positive: 0; Negative: 1; Trend: 0) |
Source |
Literature |

SNP related association results

SNP related genes (count: 3)

SNPs in LD with rs10482605 (count: 0)

SNP related eQTL (count: 1)