SNP Report

Basic Info
Name |
rs10768754
dbSNP
Ensembl
|
Location |
11:41802383 - 41802383(+) |
Variant Seq |
C |
Ancestral Allele |
C |
Ref Seq |
T |
Minor Allele Frequence |
0.441494 |
Annotation |
downstream_gene_variant; intron_variant; non_coding_transcript_variant
|
Variant Effect |
downstream_gene_variant(ENST00000531247); intron_variant(ENST00000529282, ENST00000528720); non_coding_transcript_variant(ENST00000529282, ENST00000528720)
|
SIFT Annotation |
tolerated
|
SIFT Variant Effect |
tolerated(ENST00000527150, ENST00000278198, ENST00000530763, ENST00000619527, ENST00000528697)
|
PolyPhen Annotation |
benign
|
PolyPhen Variant Effect |
benign(ENST00000527150, ENST00000278198, ENST00000530763, ENST00000619527, ENST00000528697)
|
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 rs10768754 (count: 0)

SNP related eQTL (count: 1)