SNP Report

Basic Info
| Name |
rs34565033
dbSNP
Ensembl
|
| Location |
5:168452122 - 168452122(+) |
| Variant Seq |
C |
| Ancestral Allele |
T |
| Ref Seq |
T |
| Minor Allele Frequence |
0.253195 |
| Annotation |
intron_variant; non_coding_transcript_variant
|
| Variant Effect |
intron_variant(ENST00000521089, ENST00000619752, ENST00000265293, ENST00000524093, ENST00000522140, ENST00000524228, ENST00000524038, ENST00000393895); non_coding_transcript_variant(ENST00000524093, ENST00000522140)
|
| SIFT Annotation |
deleterious
|
| SIFT Variant Effect |
deleterious(ENST00000524038, ENST00000393895, ENST00000619752, ENST00000265293, ENST00000524228, ENST00000521089)
|
| PolyPhen Annotation |
benign; possibly_damaging; probably_damaging
|
| PolyPhen Variant Effect |
benign(ENST00000393895); possibly_damaging(ENST00000619752, ENST00000265293, ENST00000524228, ENST00000521089); probably_damaging(ENST00000524038)
|
| rSNP? |
Yes
Link in rVarBase
|
| Related Regulatory Elements |
n/a
|
| Chromatin State |
Weak transcription;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: 1)

SNPs in LD with rs34565033 (count: 0)

SNP related eQTL (count: 1)