SNP Report

Basic Info
Name |
rs1478273
dbSNP
Ensembl
|
Location |
8:4610666 - 4610666(+) |
Variant Seq |
G |
Ancestral Allele |
G |
Ref Seq |
C |
Minor Allele Frequence |
0.475639 |
Annotation |
intron_variant
|
Variant Effect |
intron_variant(ENST00000520002, ENST00000400186, ENST00000602723, ENST00000635120, ENST00000602557)
|
SIFT Annotation |
tolerated
|
SIFT Variant Effect |
tolerated(ENST00000520002, ENST00000602723, ENST00000635120, ENST00000602557, ENST00000400186)
|
PolyPhen Annotation |
benign
|
PolyPhen Variant Effect |
benign(ENST00000520002, ENST00000602723, ENST00000635120, ENST00000602557, ENST00000400186)
|
rSNP? |
No
Link in rVarBase
|
Related Regulatory Elements |
n/a
|
Chromatin State |
Inactive region
|
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 rs1478273 (count: 0)

SNP related eQTL (count: 1)