SNP Report

Basic Info
Name |
rs17689378
dbSNP
Ensembl
|
Location |
17:45804424 - 45804424(+) |
Variant Seq |
T |
Ancestral Allele |
C |
Ref Seq |
C |
Minor Allele Frequence |
0.0864617 |
Annotation |
upstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant
|
Variant Effect |
upstream_gene_variant(ENST00000580955); intron_variant(ENST00000352855, ENST00000582766, ENST00000398285, ENST00000347197, ENST00000587305, ENST00000293493, ENST00000339069, ENST00000634540, ENST00000619154, ENST00000314537, ENST00000577353, ENST00000634876); NMD_transcript_variant(ENST00000347197); non_coding_transcript_variant(ENST00000582766, ENST00000587305, ENST00000634876)
|
SIFT Annotation |
deleterious_-_low_confidence; tolerated_-_low_confidence; tolerated
|
SIFT Variant Effect |
deleterious_-_low_confidence(ENST00000619154); tolerated_-_low_confidence(ENST00000352855, ENST00000293493, ENST00000347197, ENST00000398285); tolerated(ENST00000314537, ENST00000577353)
|
PolyPhen Annotation |
unknown; benign
|
PolyPhen Variant Effect |
unknown(ENST00000619154); benign(ENST00000314537, ENST00000352855, ENST00000293493, ENST00000577353, ENST00000347197, ENST00000398285)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
TF binding region;Chromatin interactive region
|
Chromatin State |
Enhancers;Weak transcription;Bivalent Enhancer
|
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 rs17689378 (count: 0)

SNP related eQTL (count: 1)