SNP Report

Basic Info
| Name |
rs71534169
dbSNP
Ensembl
|
| Location |
7:154801156 - 154801156(+) |
| Variant Seq |
G |
| Ancestral Allele |
T |
| Ref Seq |
T |
| Minor Allele Frequence |
0.0191693 |
| Annotation |
downstream_gene_variant; upstream_gene_variant; intron_variant; non_coding_transcript_variant
|
| Variant Effect |
downstream_gene_variant(ENST00000481593, ENST00000634859); upstream_gene_variant(ENST00000493268, ENST00000634717); intron_variant(ENST00000332007, ENST00000634466, ENST00000427557, ENST00000635128, ENST00000634779, ENST00000634541, ENST00000471100, ENST00000377770, ENST00000634521, ENST00000404039); non_coding_transcript_variant(ENST00000471100, ENST00000634521)
|
| SIFT Annotation |
tolerated
|
| SIFT Variant Effect |
tolerated(ENST00000404039, ENST00000634466, ENST00000634541, ENST00000427557, ENST00000332007, ENST00000634779, ENST00000377770, ENST00000635128)
|
| PolyPhen Annotation |
probably_damaging; possibly_damaging
|
| PolyPhen Variant Effect |
probably_damaging(ENST00000634466, ENST00000427557, ENST00000332007, ENST00000634779); possibly_damaging(ENST00000404039, ENST00000634541, ENST00000377770, ENST00000635128)
|
| rSNP? |
Yes
Link in rVarBase
|
| Related Regulatory Elements |
TF binding region
|
| Chromatin State |
Weak transcription
|
| No. of Marker's Association Results |
1 (Positive: 0; Negative: 0; Trend: 1) |
| Source |
Literature |

SNP related association results

SNP related genes (count: 1)

SNPs in LD with rs71534169 (count: 0)

SNP related eQTL (count: 1)