SNP Report
Name | rs2108977 dbSNP Ensembl | ||
---|---|---|---|
Location | 11:18019049 - 18019049(+) | ||
Variant Seq | C | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.437101 | ||
Annotation | downstream_gene_variant; 3_prime_UTR_variant; intron_variant; non_coding_transcript_variant | ||
Variant Effect | downstream_gene_variant(ENST00000417164, ENST00000525406); 3_prime_UTR_variant(ENST00000250018); intron_variant(ENST00000525523); non_coding_transcript_variant(ENST00000525523) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000250018) | ||
PolyPhen Annotation | possibly_damaging | ||
PolyPhen Variant Effect | possibly_damaging(ENST00000250018) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature |
The LD data used here is based on 1000 Genome Phase I. LD SNP pairs were selected with a threshold r2<=0.8.