SNP Report

Basic Info
| Name |
rs211135
dbSNP
Ensembl
|
| Location |
11:18002420 - 18002420(+) |
| Variant Seq |
A |
| Ancestral Allele |
C |
| Ref Seq |
C |
| Minor Allele Frequence |
0.463458 |
| Annotation |
upstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant
|
| Variant Effect |
upstream_gene_variant(ENST00000529151); intron_variant(ENST00000527494, ENST00000524716, ENST00000532389, ENST00000525523, ENST00000532212, ENST00000533328, ENST00000532265, ENST00000529728, ENST00000525422, ENST00000528200, ENST00000265965, ENST00000530925, ENST00000530613, ENST00000525920); NMD_transcript_variant(ENST00000527494, ENST00000524716, ENST00000533328, ENST00000525422, ENST00000530925); non_coding_transcript_variant(ENST00000525523, ENST00000532212)
|
| SIFT Annotation |
tolerated
|
| SIFT Variant Effect |
tolerated(ENST00000525422, ENST00000265965, ENST00000528200)
|
| PolyPhen Annotation |
possibly_damaging; probably_damaging
|
| PolyPhen Variant Effect |
possibly_damaging(ENST00000265965, ENST00000528200); probably_damaging(ENST00000525422)
|
| rSNP? |
Yes
Link in rVarBase
|
| Related Regulatory Elements |
n/a
|
| Chromatin State |
Weak transcription;Strong transcription;Genic 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: 1)

SNPs in LD with rs211135 (count: 0)

SNP related eQTL (count: 1)