SNP Report

Basic Info
Name |
rs62056778
dbSNP
Ensembl
|
Location |
17:45894238 - 45894238(+) |
Variant Seq |
G |
Ancestral Allele |
G |
Ref Seq |
C |
Minor Allele Frequence |
0.0860623 |
Annotation |
upstream_gene_variant; intron_variant; non_coding_transcript_variant
|
Variant Effect |
upstream_gene_variant(ENST00000624111, ENST00000535772, ENST00000334239, ENST00000570299, ENST00000344290, ENST00000262410, ENST00000571311, ENST00000351559, ENST00000446361, ENST00000340799); intron_variant(ENST00000634876, ENST00000579599, ENST00000579244); non_coding_transcript_variant(ENST00000634876, ENST00000579599, ENST00000579244)
|
SIFT Annotation |
tolerated
|
SIFT Variant Effect |
tolerated(ENST00000329196)
|
PolyPhen Annotation |
benign
|
PolyPhen Variant Effect |
benign(ENST00000329196)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
TF binding region;Chromatin interactive region
|
Chromatin State |
Bivalent/Poised TSS;Active TSS;Flanking Bivalent TSS/Enh;Flanking Active TSS;Enhancers;Weak transcription;Transcr. at gene 5' nd 3'
|
No. of Marker's Association Results |
0 (Positive: 0; Negative: 0; Trend: 0) |
Source |
LD-proxy |

SNP related association results

SNP related genes (count: 5)

SNPs in LD with rs62056778 (count: 0)

SNP related eQTL (count: 1)