SNP Report
Name | rs6912833 dbSNP Ensembl | ||
---|---|---|---|
Location | 6:35649808 - 35649808(+) | ||
Variant Seq | T | ||
Ancestral Allele | T | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.219848 | ||
Annotation | upstream_gene_variant; intron_variant | ||
Variant Effect | upstream_gene_variant(ENST00000391277); intron_variant(ENST00000357266, ENST00000536438, ENST00000539068, ENST00000542713) | ||
SIFT Annotation | deleterious; tolerated | ||
SIFT Variant Effect | deleterious(ENST00000542713); tolerated(ENST00000539068, ENST00000357266, ENST00000536438) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000539068, ENST00000542713, ENST00000357266, ENST00000536438) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | TF binding region;Chromatin interactive region | ||
Chromatin State | Weak transcription;Strong transcription;Genic enhancers;Enhancers | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |