SNP Report

Basic Info
Name |
rs2251177
dbSNP
Ensembl
|
Location |
3:114139503 - 114139503(+) |
Variant Seq |
A,T |
Ancestral Allele |
T |
Ref Seq |
C |
Minor Allele Frequence |
0.0421326 |
Annotation |
synonymous_variant; missense_variant
|
Variant Effect |
synonymous_variant(ENST00000295881, ENST00000460779, ENST00000467632, ENST00000383673); missense_variant(ENST00000295881, ENST00000460779, ENST00000467632, ENST00000383673)
|
SIFT Annotation |
tolerated
|
SIFT Variant Effect |
tolerated(ENST00000295881, ENST00000460779, ENST00000467632, ENST00000383673)
|
PolyPhen Annotation |
benign
|
PolyPhen Variant Effect |
benign(ENST00000295881, ENST00000460779, ENST00000467632, ENST00000383673)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
n/a
|
Chromatin State |
Enhancers
|
No. of Marker's Association Results |
1 (Positive: 1; Negative: 0; Trend: 0) |
Source |
Literature |

SNP related association results

SNP related genes (count: 1)

SNPs in LD with rs2251177 (count: 0)

SNP related eQTL (count: 1)