SNP Report
Name | rs4713899 dbSNP Ensembl | ||
---|---|---|---|
Location | 6:35601504 - 35601504(+) | ||
Variant Seq | G | ||
Ancestral Allele | G | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.164137 | ||
Annotation | intron_variant | ||
Variant Effect | intron_variant(ENST00000542713, ENST00000539068, ENST00000357266, ENST00000536438) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000357266, ENST00000539068, ENST00000536438) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000357266, ENST00000539068, ENST00000536438) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Enhancers;Weak transcription;Flanking Active TSS;Active TSS;Bivalent Enhancer | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |