SNP Report
Name | rs1386485 dbSNP Ensembl | ||
---|---|---|---|
Location | 12:72018587 - 72018587(+) | ||
Variant Seq | T | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.463858 | ||
Annotation | intron_variant | ||
Variant Effect | intron_variant(ENST00000333850) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000333850) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000333850) | ||
rSNP? | No Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Inactive region | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |