SNP Report

Basic Info
Name |
rs17670544
dbSNP
Ensembl
|
Location |
16:9986175 - 9986175(+) |
Variant Seq |
T |
Ancestral Allele |
A |
Ref Seq |
A |
Minor Allele Frequence |
0.0509185 |
Annotation |
intron_variant; non_coding_transcript_variant
|
Variant Effect |
intron_variant(ENST00000568247, ENST00000566683, ENST00000562109, ENST00000330684, ENST00000566670, ENST00000396573); non_coding_transcript_variant(ENST00000568247, ENST00000566683, ENST00000566670)
|
SIFT Annotation |
tolerated
|
SIFT Variant Effect |
tolerated(ENST00000396573, ENST00000330684, ENST00000396575, ENST00000562109, ENST00000535259)
|
PolyPhen Annotation |
benign; probably_damaging
|
PolyPhen Variant Effect |
benign(ENST00000396573, ENST00000330684, ENST00000562109, ENST00000535259); probably_damaging(ENST00000396575)
|
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 rs17670544 (count: 0)

SNP related eQTL (count: 1)