SNP Report

Basic Info
Name |
rs157595
dbSNP
Ensembl
|
Location |
19:44922203 - 44922203(+) |
Variant Seq |
G |
Ref Seq |
A |
Minor Allele Frequence |
0.400759 |
Annotation |
downstream_gene_variant; upstream_gene_variant
|
Variant Effect |
downstream_gene_variant(ENST00000588750, ENST00000592535, ENST00000589781, ENST00000590334, ENST00000586638, ENST00000592176, ENST00000592885, ENST00000588802); upstream_gene_variant(ENST00000575148, ENST00000571466, ENST00000574565, ENST00000589081, ENST00000507983)
|
SIFT Annotation |
tolerated_-_low_confidence; deleterious_-_low_confidence; deleterious; tolerated
|
SIFT Variant Effect |
tolerated_-_low_confidence(ENST00000589078); deleterious_-_low_confidence(ENST00000592885, ENST00000586638, ENST00000590334); deleterious(ENST00000592535); tolerated(ENST00000588802, ENST00000588750)
|
PolyPhen Annotation |
benign
|
PolyPhen Variant Effect |
benign(ENST00000592885, ENST00000588802, ENST00000589078, ENST00000586638, ENST00000590334, ENST00000592535, ENST00000588750)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
Chromatin interactive region
|
Chromatin State |
Weak transcription;Enhancers
|
No. of Marker's Association Results |
0 (Positive: 0; Negative: 0; Trend: 0) |
Source |
LD-proxy |

SNP related association results

SNP related genes (count: 3)

SNPs in LD with rs157595 (count: 0)

SNP related eQTL (count: 1)