SNP Report

Basic Info
| Name |
rs10268647
dbSNP
Ensembl
|
| Location |
7:31075262 - 31075262(+) |
| Variant Seq |
G |
| Ancestral Allele |
A |
| Ref Seq |
A |
| Minor Allele Frequence |
0.0716853 |
| Annotation |
intron_variant
|
| Variant Effect |
intron_variant(ENST00000409489, ENST00000396211, ENST00000431811, ENST00000614107, ENST00000409363, ENST00000304166)
|
| SIFT Annotation |
tolerated_-_low_confidence; tolerated
|
| SIFT Variant Effect |
tolerated_-_low_confidence(ENST00000409489, ENST00000304166, ENST00000614107, ENST00000396211, ENST00000409363); tolerated(ENST00000431811)
|
| PolyPhen Annotation |
benign
|
| PolyPhen Variant Effect |
benign(ENST00000409489, ENST00000304166, ENST00000614107, ENST00000431811, ENST00000396211, ENST00000409363)
|
| rSNP? |
Yes
Link in rVarBase
|
| Related Regulatory Elements |
n/a
|
| Chromatin State |
Weak transcription;Strong transcription;Enhancers;Genic enhancers;Bivalent Enhancer
|
| 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 rs10268647 (count: 0)

SNP related eQTL (count: 1)