SNP Report

Basic Info
| Name |
rs406744
dbSNP
Ensembl
|
| Location |
11:41814576 - 41814576(+) |
| Variant Seq |
G |
| Ancestral Allele |
G |
| Ref Seq |
T |
| Minor Allele Frequence |
0.488818 |
| Annotation |
intron_variant; non_coding_transcript_variant
|
| Variant Effect |
intron_variant(ENST00000528720, ENST00000529282); non_coding_transcript_variant(ENST00000528720, ENST00000529282)
|
| SIFT Annotation |
tolerated
|
| SIFT Variant Effect |
tolerated(ENST00000527150, ENST00000278198, ENST00000530763, ENST00000619527, ENST00000528697)
|
| PolyPhen Annotation |
benign
|
| PolyPhen Variant Effect |
benign(ENST00000527150, ENST00000278198, ENST00000530763, ENST00000619527, ENST00000528697)
|
| rSNP? |
No
Link in rVarBase
|
| Related Regulatory Elements |
n/a
|
| Chromatin State |
Inactive region
|
| 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 rs406744 (count: 0)

SNP related eQTL (count: 1)