SNP Report
Name | rs1500899 dbSNP Ensembl | ||
---|---|---|---|
Location | 8:95522762 - 95522762(+) | ||
Variant Seq | T | ||
Ancestral Allele | T | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.297125 | ||
Annotation | intron_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000517437, ENST00000519366, ENST00000521905); non_coding_transcript_variant(ENST00000517437, ENST00000519366, ENST00000521905) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000286688) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000286688) | ||
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 |