SNP Report
Name | rs11606304 dbSNP Ensembl | ||
---|---|---|---|
Location | 11:18030701 - 18030701(+) | ||
Variant Seq | G | ||
Ancestral Allele | T | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.0283546 | ||
Annotation | intron_variant; NMD_transcript_variant | ||
Variant Effect | intron_variant(ENST00000417164, ENST00000528338, ENST00000250018); NMD_transcript_variant(ENST00000417164) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000250018) | ||
PolyPhen Annotation | probably_damaging | ||
PolyPhen Variant Effect | probably_damaging(ENST00000250018) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 2 (Positive: 0; Negative: 2; Trend: 0) | ||
Source | Literature |