SNP Report

Basic Info
Name |
rs4923457
dbSNP
Ensembl
|
Location |
11:27627033 - 27627033(+) |
Variant Seq |
T |
Ancestral Allele |
G |
Ref Seq |
A |
Minor Allele Frequence |
0.252396 |
Annotation |
intron_variant; non_coding_transcript_variant
|
Variant Effect |
intron_variant(ENST00000530686, ENST00000501176, ENST00000527083, ENST00000532965, ENST00000500662, ENST00000534757, ENST00000499008, ENST00000499568, ENST00000502161); non_coding_transcript_variant(ENST00000530686, ENST00000501176, ENST00000527083, ENST00000532965, ENST00000500662, ENST00000534757, ENST00000499008, ENST00000499568, ENST00000502161)
|
SIFT Annotation |
tolerated_-_low_confidence
|
SIFT Variant Effect |
tolerated_-_low_confidence(ENST00000278193, ENST00000524596)
|
PolyPhen Annotation |
benign
|
PolyPhen Variant Effect |
benign(ENST00000278193, ENST00000524596)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
n/a
|
Chromatin State |
Enhancers;Weak transcription;Genic enhancers;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: 2)

SNPs in LD with rs4923457 (count: 0)

SNP related eQTL (count: 1)