SNP Report
Name | rs685657 dbSNP Ensembl | ||
---|---|---|---|
Location | 11:18039122 - 18039122(+) | ||
Variant Seq | T | ||
Ancestral Allele | C | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.305112 | ||
Annotation | intron_variant; NMD_transcript_variant | ||
Variant Effect | intron_variant(ENST00000528338, ENST00000417164, ENST00000250018); NMD_transcript_variant(ENST00000417164) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000250018, ENST00000417164, ENST00000528338) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000250018, ENST00000417164, ENST00000528338) | ||
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 |