SNP Report

Basic Info
| Name |
rs2267710
dbSNP
Ensembl
|
| Location |
7:30656574 - 30656574(+) |
| Variant Seq |
T |
| Ancestral Allele |
C |
| Ref Seq |
C |
| Minor Allele Frequence |
0.413538 |
| Annotation |
intron_variant; NMD_transcript_variant
|
| Variant Effect |
intron_variant(ENST00000452278, ENST00000341843, ENST00000348438, ENST00000471646, ENST00000506074); NMD_transcript_variant(ENST00000452278)
|
| SIFT Annotation |
tolerated
|
| SIFT Variant Effect |
tolerated(ENST00000471646, ENST00000506074, ENST00000348438, ENST00000341843)
|
| PolyPhen Annotation |
benign
|
| PolyPhen Variant Effect |
benign(ENST00000471646, ENST00000506074, ENST00000348438, ENST00000341843)
|
| rSNP? |
Yes
Link in rVarBase
|
| Related Regulatory Elements |
n/a
|
| Chromatin State |
Weak transcription;Strong transcription;Bivalent Enhancer
|
| 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 rs2267710 (count: 0)

SNP related eQTL (count: 1)