SNP Report
Name | rs10891546 dbSNP Ensembl | ||
---|---|---|---|
Location | 11:113394570 - 113394570(+) | ||
Variant Seq | C | ||
Ancestral Allele | C | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.473243 | ||
Annotation | intron_variant; NMD_transcript_variant | ||
Variant Effect | intron_variant(ENST00000303941, ENST00000542948); NMD_transcript_variant(ENST00000542948) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000303941, ENST00000542948) | ||
PolyPhen Annotation | possibly_damaging | ||
PolyPhen Variant Effect | possibly_damaging(ENST00000303941, ENST00000542948) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Strong transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |