SNP Report

Basic Info
Name |
rs1081105
dbSNP
Ensembl
|
Location |
19:44909698 - 44909698(+) |
Variant Seq |
C |
Ancestral Allele |
A |
Ref Seq |
A |
Minor Allele Frequence |
0.0301518 |
Annotation |
downstream_gene_variant; non_coding_transcript_exon_variant; upstream_gene_variant; non_coding_transcript_variant
|
Variant Effect |
downstream_gene_variant(ENST00000485628, ENST00000446996, ENST00000434152, ENST00000425718, ENST00000252486); non_coding_transcript_exon_variant(ENST00000623895); upstream_gene_variant(ENST00000588750, ENST00000588802, ENST00000592535); non_coding_transcript_variant(ENST00000623895)
|
SIFT Annotation |
deleterious_-_low_confidence; tolerated_-_low_confidence; tolerated
|
SIFT Variant Effect |
deleterious_-_low_confidence(ENST00000592885); tolerated_-_low_confidence(ENST00000589078, ENST00000586638, ENST00000590334); tolerated(ENST00000592535, ENST00000588802, ENST00000588750)
|
PolyPhen Annotation |
unknown; probably_damaging
|
PolyPhen Variant Effect |
unknown(ENST00000589781, ENST00000592176); probably_damaging(ENST00000589078, ENST00000586638, ENST00000592535, ENST00000590334, ENST00000588802, ENST00000592885, ENST00000588750)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
TF binding region;Chromatin interactive region
|
Chromatin State |
Weak transcription;Strong transcription;Enhancers;Active TSS;Genic enhancers
|
No. of Marker's Association Results |
1 (Positive: 0; Negative: 1; Trend: 0) |
Source |
Literature |

SNP related association results

SNP related genes (count: 3)

SNPs in LD with rs1081105 (count: 0)

SNP related eQTL (count: 1)