SNP Report

Basic Info
| Name |
rs79590198
dbSNP
Ensembl
|
| Location |
5:143307371 - 143307371(+) |
| Variant Seq |
A |
| Ancestral Allele |
G |
| Ref Seq |
G |
| Minor Allele Frequence |
0.0509185 |
| Annotation |
intron_variant; non_coding_transcript_variant
|
| Variant Effect |
intron_variant(ENST00000503201, ENST00000504336, ENST00000504572, ENST00000394464, ENST00000343796, ENST00000424646, ENST00000231509, ENST00000394466, ENST00000415690); non_coding_transcript_variant(ENST00000504336)
|
| SIFT Annotation |
deleterious
|
| SIFT Variant Effect |
deleterious(ENST00000394464, ENST00000503201, ENST00000415690, ENST00000424646, ENST00000231509, ENST00000343796, ENST00000504572, ENST00000394466)
|
| PolyPhen Annotation |
probably_damaging
|
| PolyPhen Variant Effect |
probably_damaging(ENST00000394464, ENST00000503201, ENST00000415690, ENST00000424646, ENST00000231509, ENST00000343796, ENST00000504572, ENST00000394466)
|
| rSNP? |
Yes
Link in rVarBase
|
| Related Regulatory Elements |
n/a
|
| Chromatin State |
Weak transcription;Strong transcription;ZNF genes & repeats
|
| No. of Marker's Association Results |
1 (Positive: 0; Negative: 1; Trend: 0) |
| Source |
Literature |

SNP related association results

SNP related genes (count: 1)

SNPs in LD with rs79590198 (count: 0)

SNP related eQTL (count: 1)