SNP Report

Basic Info
Name |
rs79590198
dbSNP
Ensembl
|
Location |
5:143307371 - 143307371(+) |
Variant Seq |
A |
Ancestral Allele |
G |
Ref Seq |
G |
Minor Allele Frequence |
0.0509185 |
Annotation |
intron_variant; non_coding_transcript_variant
|
Variant Effect |
intron_variant(ENST00000503201, ENST00000504336, ENST00000504572, ENST00000394464, ENST00000343796, ENST00000424646, ENST00000231509, ENST00000394466, ENST00000415690); non_coding_transcript_variant(ENST00000504336)
|
SIFT Annotation |
deleterious
|
SIFT Variant Effect |
deleterious(ENST00000394464, ENST00000503201, ENST00000415690, ENST00000424646, ENST00000231509, ENST00000343796, ENST00000504572, ENST00000394466)
|
PolyPhen Annotation |
probably_damaging
|
PolyPhen Variant Effect |
probably_damaging(ENST00000394464, ENST00000503201, ENST00000415690, ENST00000424646, ENST00000231509, ENST00000343796, ENST00000504572, ENST00000394466)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
n/a
|
Chromatin State |
Weak transcription;Strong transcription;ZNF genes & repeats
|
No. of Marker's Association Results |
1 (Positive: 0; Negative: 1; Trend: 0) |
Source |
Literature |

SNP related association results

SNP related genes (count: 1)

SNPs in LD with rs79590198 (count: 0)

SNP related eQTL (count: 1)