SNP Report

Basic Info
Name |
rs11076111
dbSNP
Ensembl
|
Location |
16:55660639 - 55660639(+) |
Variant Seq |
C |
Ancestral Allele |
C |
Ref Seq |
G |
Minor Allele Frequence |
0.247404 |
Annotation |
intron_variant
|
Variant Effect |
intron_variant(ENST00000379906, ENST00000219833, ENST00000568655, ENST00000568529, ENST00000568943, ENST00000414754, ENST00000566163, ENST00000561820)
|
SIFT Annotation |
deleterious; tolerated
|
SIFT Variant Effect |
deleterious(ENST00000561820, ENST00000414754, ENST00000379906, ENST00000568943); tolerated(ENST00000219833, ENST00000561820, ENST00000568655, ENST00000379906, ENST00000566163, ENST00000568529, ENST00000568943)
|
PolyPhen Annotation |
benign; possibly_damaging
|
PolyPhen Variant Effect |
benign(ENST00000219833, ENST00000561820, ENST00000414754, ENST00000568655, ENST00000379906, ENST00000566163, ENST00000568529, ENST00000568943); possibly_damaging(ENST00000414754)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
n/a
|
Chromatin State |
Weak transcription;Enhancers;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: 1)

SNPs in LD with rs11076111 (count: 0)

SNP related eQTL (count: 1)