SNP Report

Basic Info
| Name |
rs6191
dbSNP
Ensembl
|
| Location |
5:143278591 - 143278591(+) |
| Variant Seq |
A |
| Ancestral Allele |
A |
| Ref Seq |
C |
| Minor Allele Frequence |
0.401558 |
| Annotation |
downstream_gene_variant; 3_prime_UTR_variant
|
| Variant Effect |
downstream_gene_variant(ENST00000424646, ENST00000504572, ENST00000394466, ENST00000231509, ENST00000503201); 3_prime_UTR_variant(ENST00000415690, ENST00000394464, ENST00000343796)
|
| SIFT Annotation |
tolerated
|
| SIFT Variant Effect |
tolerated(ENST00000378004, ENST00000418236, ENST00000443674, ENST00000274498)
|
| PolyPhen Annotation |
benign; possibly_damaging
|
| PolyPhen Variant Effect |
benign(ENST00000378004, ENST00000418236); possibly_damaging(ENST00000443674, ENST00000274498)
|
| rSNP? |
Yes
Link in rVarBase
|
| Related Regulatory Elements |
n/a
|
| Chromatin State |
Weak transcription;Enhancers;Strong transcription;Genic enhancers
|
| 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 rs6191 (count: 0)

SNP related eQTL (count: 1)