SNP Report

Basic Info
| Name |
rs1437545
dbSNP
Ensembl
|
| Location |
15:61193643 - 61193643(+) |
| Variant Seq |
C |
| Ancestral Allele |
A |
| Ref Seq |
A |
| Minor Allele Frequence |
0.247404 |
| Annotation |
intron_variant; NMD_transcript_variant; non_coding_transcript_variant
|
| Variant Effect |
intron_variant(ENST00000559145, ENST00000560300, ENST00000557822, ENST00000560876, ENST00000561093, ENST00000558904, ENST00000551975, ENST00000335670); NMD_transcript_variant(ENST00000551975); non_coding_transcript_variant(ENST00000559145, ENST00000560300, ENST00000557822, ENST00000560876, ENST00000561093)
|
| SIFT Annotation |
deleterious_-_low_confidence; tolerated
|
| SIFT Variant Effect |
deleterious_-_low_confidence(ENST00000551975); tolerated(ENST00000335670)
|
| PolyPhen Annotation |
benign; possibly_damaging
|
| PolyPhen Variant Effect |
benign(ENST00000335670); possibly_damaging(ENST00000551975)
|
| rSNP? |
Yes
Link in rVarBase
|
| Related Regulatory Elements |
n/a
|
| Chromatin State |
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 rs1437545 (count: 0)

SNP related eQTL (count: 1)