SNP Report

Basic Info
| Name |
rs78826942
dbSNP
Ensembl
|
| Location |
15:44103716 - 44103716(+) |
| Variant Seq |
C |
| Ancestral Allele |
T |
| Ref Seq |
T |
| Minor Allele Frequence |
0.01877 |
| Annotation |
intron_variant; NMD_transcript_variant
|
| Variant Effect |
intron_variant(ENST00000421674, ENST00000451277, ENST00000484674, ENST00000417257, ENST00000402883, ENST00000458630); NMD_transcript_variant(ENST00000421674, ENST00000451277, ENST00000458630)
|
| SIFT Annotation |
deleterious
|
| SIFT Variant Effect |
deleterious(ENST00000421674, ENST00000449926, ENST00000402883, ENST00000451277, ENST00000458630, ENST00000417257)
|
| PolyPhen Annotation |
probably_damaging
|
| PolyPhen Variant Effect |
probably_damaging(ENST00000421674, ENST00000449926, ENST00000402883, ENST00000451277, ENST00000458630, ENST00000417257)
|
| rSNP? |
Yes
Link in rVarBase
|
| Related Regulatory Elements |
n/a
|
| Chromatin State |
Weak transcription;Bivalent Enhancer;Enhancers
|
| No. of Marker's Association Results |
1 (Positive: 0; Negative: 0; Trend: 1) |
| Source |
Literature |

SNP related association results

SNP related genes (count: 1)

SNPs in LD with rs78826942 (count: 0)

SNP related eQTL (count: 1)