SNP Report

Basic Info
| Name |
rs61938733
dbSNP
Ensembl
|
| Location |
12:117349366 - 117349366(+) |
| Variant Seq |
A |
| Ancestral Allele |
G |
| Ref Seq |
G |
| Minor Allele Frequence |
0.0155751 |
| Annotation |
intron_variant; non_coding_transcript_variant
|
| Variant Effect |
intron_variant(ENST00000618760, ENST00000549189, ENST00000317775, ENST00000477584); non_coding_transcript_variant(ENST00000549189, ENST00000477584)
|
| SIFT Annotation |
deleterious_-_low_confidence
|
| SIFT Variant Effect |
deleterious_-_low_confidence(ENST00000317775, ENST00000338101, ENST00000618760, ENST00000344089)
|
| PolyPhen Annotation |
probably_damaging
|
| PolyPhen Variant Effect |
probably_damaging(ENST00000317775, ENST00000338101, ENST00000618760, ENST00000344089)
|
| rSNP? |
Yes
Link in rVarBase
|
| Related Regulatory Elements |
n/a
|
| Chromatin State |
Weak transcription;Enhancers
|
| 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 rs61938733 (count: 0)

SNP related eQTL (count: 1)