SNP Report

Basic Info
| Name |
rs61012457
dbSNP
Ensembl
|
| Location |
15:78573352 - 78573352(+) |
| Variant Seq |
G |
| Ancestral Allele |
C |
| Ref Seq |
C |
| Minor Allele Frequence |
0.205671 |
| Annotation |
intron_variant
|
| Variant Effect |
intron_variant(ENST00000559554, ENST00000299565)
|
| SIFT Annotation |
tolerated
|
| SIFT Variant Effect |
tolerated(ENST00000044462, ENST00000413382, ENST00000559154, ENST00000559948, ENST00000559365, ENST00000560217, ENST00000559082, ENST00000560737, ENST00000558094, ENST00000558281, ENST00000559437, ENST00000559146)
|
| PolyPhen Annotation |
benign
|
| PolyPhen Variant Effect |
benign(ENST00000044462, ENST00000413382, ENST00000559154, ENST00000559948, ENST00000559365, ENST00000560217, ENST00000559082, ENST00000560737, ENST00000558094, ENST00000558281, ENST00000559437, ENST00000559146)
|
| rSNP? |
Yes
Link in rVarBase
|
| Related Regulatory Elements |
Chromatin interactive region
|
| Chromatin State |
ZNF genes & repeats;Weak 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: 1)

SNPs in LD with rs61012457 (count: 0)

SNP related eQTL (count: 1)