SNP Report
Name | rs139604943 dbSNP Ensembl | ||
---|---|---|---|
Location | 10:60652713 - 60652713(+) | ||
Variant Seq | T | ||
Ancestral Allele | A | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.0125799 | ||
Annotation | intron_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000373827, ENST00000510382); non_coding_transcript_variant(ENST00000510382) | ||
SIFT Annotation | tolerated_-_low_confidence | ||
SIFT Variant Effect | tolerated_-_low_confidence(ENST00000373827) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000373827) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Weak transcription;Enhancers | ||
No. of Marker's Association Results | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature |