SNP Report

Basic Info
| Name |
rs4923457
dbSNP
Ensembl
|
| Location |
11:27627033 - 27627033(+) |
| Variant Seq |
T |
| Ancestral Allele |
G |
| Ref Seq |
A |
| Minor Allele Frequence |
0.252396 |
| Annotation |
intron_variant; non_coding_transcript_variant
|
| Variant Effect |
intron_variant(ENST00000530686, ENST00000501176, ENST00000527083, ENST00000532965, ENST00000500662, ENST00000534757, ENST00000499008, ENST00000499568, ENST00000502161); non_coding_transcript_variant(ENST00000530686, ENST00000501176, ENST00000527083, ENST00000532965, ENST00000500662, ENST00000534757, ENST00000499008, ENST00000499568, ENST00000502161)
|
| SIFT Annotation |
tolerated_-_low_confidence
|
| SIFT Variant Effect |
tolerated_-_low_confidence(ENST00000278193, ENST00000524596)
|
| PolyPhen Annotation |
benign
|
| PolyPhen Variant Effect |
benign(ENST00000278193, ENST00000524596)
|
| rSNP? |
Yes
Link in rVarBase
|
| Related Regulatory Elements |
n/a
|
| Chromatin State |
Enhancers;Weak transcription;Genic enhancers;Strong transcription
|
| No. of Marker's Association Results |
0 (Positive: 0; Negative: 0; Trend: 0) |
| Source |
LD-proxy |

SNP related association results

SNP related genes (count: 2)

SNPs in LD with rs4923457 (count: 0)

SNP related eQTL (count: 1)