SNP Report

Basic Info
Name |
rs61586133
dbSNP
Ensembl
|
Location |
8:27508659 - 27508659(+) |
Variant Seq |
A |
Ancestral Allele |
G |
Ref Seq |
G |
Minor Allele Frequence |
0.0123802 |
Annotation |
downstream_gene_variant; intron_variant; non_coding_transcript_variant
|
Variant Effect |
downstream_gene_variant(ENST00000520666, ENST00000518328, ENST00000523827); intron_variant(ENST00000521400, ENST00000380476, ENST00000521780, ENST00000521924, ENST00000520623, ENST00000521684, ENST00000518379, ENST00000517536); non_coding_transcript_variant(ENST00000521924, ENST00000520623)
|
SIFT Annotation |
deleterious
|
SIFT Variant Effect |
deleterious(ENST00000518379, ENST00000380476, ENST00000521684, ENST00000521780, ENST00000518328, ENST00000521400)
|
PolyPhen Annotation |
benign; possibly_damaging
|
PolyPhen Variant Effect |
benign(ENST00000380476, ENST00000521780, ENST00000518328, ENST00000521400); possibly_damaging(ENST00000518379, ENST00000521684)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
n/a
|
Chromatin State |
Weak transcription;Strong 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 rs61586133 (count: 0)

SNP related eQTL (count: 1)