SNP Report
Name | rs190526 dbSNP Ensembl | ||
---|---|---|---|
Location | 8:130812621 - 130812621(+) | ||
Variant Seq | T | ||
Ancestral Allele | A | ||
Ref Seq | A | ||
Annotation | intron_variant | ||
Variant Effect | intron_variant(ENST00000377928, ENST00000286355) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000377928, ENST00000286355) | ||
PolyPhen Annotation | probably_damaging; possibly_damaging | ||
PolyPhen Variant Effect | probably_damaging(ENST00000286355); possibly_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 |