SNP Report

Basic Info
Name |
rs17054232
dbSNP
Ensembl
|
Location |
4:168475606 - 168475606(+) |
Variant Seq |
A |
Ancestral Allele |
G |
Ref Seq |
G |
Minor Allele Frequence |
0.343251 |
Annotation |
downstream_gene_variant; intron_variant; non_coding_transcript_variant
|
Variant Effect |
downstream_gene_variant(ENST00000384442, ENST00000505150); intron_variant(ENST00000513901, ENST00000505696, ENST00000511577, ENST00000512371, ENST00000260184, ENST00000514748, ENST00000505890, ENST00000515088); non_coding_transcript_variant(ENST00000513901, ENST00000515088)
|
SIFT Annotation |
deleterious
|
SIFT Variant Effect |
deleterious(ENST00000505890, ENST00000260184, ENST00000511577, ENST00000514748, ENST00000512371, ENST00000505696)
|
PolyPhen Annotation |
possibly_damaging
|
PolyPhen Variant Effect |
possibly_damaging(ENST00000505890, ENST00000260184, ENST00000511577, ENST00000514748, ENST00000512371, ENST00000505696)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
Chromatin interactive region
|
Chromatin State |
Enhancers;Weak transcription;Genic enhancers
|
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 rs17054232 (count: 0)

SNP related eQTL (count: 1)