SNP Report
Name | rs1799836 dbSNP Ensembl | ||
---|---|---|---|
Location | X:43768752 - 43768752(+) | ||
Variant Seq | C | ||
Ancestral Allele | T | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.456689 | ||
Annotation | intron_variant | ||
Variant Effect | intron_variant(ENST00000378069) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000378069) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000378069) | ||
rSNP? | No Link in rVarBase | ||
Related Regulatory Elements | N.A. | ||
Chromatin State | N.A. | ||
No. of Marker's Association Results | 2 (Positive: 1; Negative: 1; Trend: 0) | ||
Source | Literature |