SNP Report

Basic Info
Name |
rs2709787
dbSNP
Ensembl
|
Location |
7:30574057 - 30574057(+) |
Variant Seq |
T |
Ancestral Allele |
T |
Ref Seq |
G |
Minor Allele Frequence |
0.188099 |
Annotation |
downstream_gene_variant; upstream_gene_variant; intron_variant; non_coding_transcript_variant
|
Variant Effect |
downstream_gene_variant(ENST00000583664, ENST00000579174, ENST00000584023, ENST00000582549, ENST00000578994, ENST00000580440, ENST00000454922); upstream_gene_variant(ENST00000579024, ENST00000614950, ENST00000582145, ENST00000584621, ENST00000584108); intron_variant(ENST00000426529, ENST00000584199, ENST00000581794, ENST00000581665, ENST00000578245, ENST00000582733, ENST00000584372); non_coding_transcript_variant(ENST00000426529, ENST00000584199, ENST00000581794, ENST00000581665, ENST00000578245, ENST00000582733, ENST00000584372)
|
SIFT Annotation |
tolerated
|
SIFT Variant Effect |
tolerated(ENST00000275428, ENST00000426081, ENST00000409436, ENST00000598361)
|
PolyPhen Annotation |
benign; probably_damaging
|
PolyPhen Variant Effect |
benign(ENST00000409436); probably_damaging(ENST00000275428, ENST00000426081, ENST00000598361)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
lncRNA
|
Chromatin State |
ZNF genes & repeats;Weak transcription;Strong 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: 0)

SNPs in LD with rs2709787 (count: 0)

SNP related eQTL (count: 1)