SNP Report

Basic Info
Name |
rs8034191
dbSNP
Ensembl
|
Location |
15:78513681 - 78513681(+) |
Variant Seq |
C |
Ancestral Allele |
T |
Ref Seq |
T |
Minor Allele Frequence |
0.188898 |
Annotation |
intron_variant; NMD_transcript_variant
|
Variant Effect |
intron_variant(ENST00000563233, ENST00000566289, ENST00000569878, ENST00000388988, ENST00000566332, ENST00000408962); NMD_transcript_variant(ENST00000566289)
|
SIFT Annotation |
tolerated
|
SIFT Variant Effect |
tolerated(ENST00000388988, ENST00000569878, ENST00000563233, ENST00000566289, ENST00000566332, ENST00000408962)
|
PolyPhen Annotation |
benign
|
PolyPhen Variant Effect |
benign(ENST00000388988, ENST00000569878, ENST00000563233, ENST00000566289, ENST00000566332, ENST00000408962)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
Chromatin interactive region
|
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: 2)

SNPs in LD with rs8034191 (count: 0)

SNP related eQTL (count: 1)