SNP Report
Name | rs1425392 dbSNP Ensembl | ||
---|---|---|---|
Location | 4:64526494 - 64526494(+) | ||
Variant Seq | C | ||
Ancestral Allele | T | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.249601 | ||
Annotation | downstream_gene_variant | ||
SIFT Annotation | tolerated_-_low_confidence; deleterious_-_low_confidence | ||
SIFT Variant Effect | tolerated_-_low_confidence(ENST00000507440, ENST00000381210); deleterious_-_low_confidence(ENST00000509536) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000509536, ENST00000507440, ENST00000381210) | ||
rSNP? | No Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Inactive region | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature |