SNP Report
Name | rs13278937 dbSNP Ensembl | ||
---|---|---|---|
Location | 8:130784244 - 130784244(+) | ||
Variant Seq | C | ||
Ancestral Allele | C | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.491613 | ||
Annotation | intron_variant | ||
Variant Effect | intron_variant(ENST00000377928, ENST00000286355) | ||
SIFT Annotation | deleterious; tolerated | ||
SIFT Variant Effect | deleterious(ENST00000377928); tolerated(ENST00000286355) | ||
PolyPhen Annotation | benign; probably_damaging | ||
PolyPhen Variant Effect | benign(ENST00000286355); probably_damaging(ENST00000377928) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |