SNP Report

Basic Info
Name |
rs11030227
dbSNP
Ensembl
|
Location |
11:28151578 - 28151578(+) |
Variant Seq |
G |
Ancestral Allele |
C |
Ref Seq |
C |
Minor Allele Frequence |
0.386581 |
Annotation |
intron_variant; NMD_transcript_variant
|
Variant Effect |
intron_variant(ENST00000634721, ENST00000634973, ENST00000634627, ENST00000406787, ENST00000451385, ENST00000407364, ENST00000303459, ENST00000532947); NMD_transcript_variant(ENST00000634973, ENST00000634627, ENST00000451385, ENST00000532947)
|
SIFT Annotation |
tolerated
|
SIFT Variant Effect |
tolerated(ENST00000437814)
|
PolyPhen Annotation |
benign
|
PolyPhen Variant Effect |
benign(ENST00000437814)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
n/a
|
Chromatin State |
Weak transcription;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 rs11030227 (count: 0)

SNP related eQTL (count: 1)