SNP Report

Basic Info
Name |
rs1541516
dbSNP
Ensembl
|
Location |
7:31082927 - 31082927(+) |
Variant Seq |
A |
Ancestral Allele |
G |
Ref Seq |
G |
Minor Allele Frequence |
0.271166 |
Annotation |
downstream_gene_variant; upstream_gene_variant; intron_variant
|
Variant Effect |
downstream_gene_variant(ENST00000431811); upstream_gene_variant(ENST00000436116); intron_variant(ENST00000409363, ENST00000304166, ENST00000409489, ENST00000396211, ENST00000614107)
|
SIFT Annotation |
deleterious; tolerated
|
SIFT Variant Effect |
deleterious(ENST00000409489, ENST00000614107, ENST00000396211); tolerated(ENST00000304166, ENST00000409363)
|
PolyPhen Annotation |
possibly_damaging; probably_damaging
|
PolyPhen Variant Effect |
possibly_damaging(ENST00000614107, ENST00000396211); probably_damaging(ENST00000409489, ENST00000304166, ENST00000409363)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
TF binding region;Chromatin interactive region
|
Chromatin State |
Weak transcription;Enhancers;Strong transcription;Bivalent Enhancer;Genic enhancers;Bivalent/Poised TSS
|
No. of Marker's Association Results |
1 (Positive: 0; Negative: 1; Trend: 0) |
Source |
Literature |

SNP related association results

SNP related genes (count: 1)

SNPs in LD with rs1541516 (count: 0)

SNP related eQTL (count: 1)