SNP Report

Basic Info
Name |
rs11979753
dbSNP
Ensembl
|
Location |
7:31091566 - 31091566(+) |
Variant Seq |
A,T |
Ancestral Allele |
A |
Ref Seq |
G |
Minor Allele Frequence |
0.123003 |
Annotation |
intron_variant
|
Variant Effect |
intron_variant(ENST00000396211, ENST00000409489, ENST00000409363, ENST00000614107, ENST00000304166, ENST00000436116)
|
SIFT Annotation |
tolerated
|
SIFT Variant Effect |
tolerated(ENST00000436116, ENST00000304166, ENST00000409489, ENST00000614107, ENST00000396211, ENST00000409363)
|
PolyPhen Annotation |
benign; possibly_damaging
|
PolyPhen Variant Effect |
benign(ENST00000436116, ENST00000304166, ENST00000409489, ENST00000409363); possibly_damaging(ENST00000614107, ENST00000396211)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
n/a
|
Chromatin State |
Weak 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: 1)

SNPs in LD with rs11979753 (count: 0)

SNP related eQTL (count: 1)