SNP Report
Name | rs10993952 dbSNP Ensembl | ||
---|---|---|---|
Location | 9:133665435 - 133665435(+) | ||
Variant Seq | T | ||
Ancestral Allele | C | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.23143 | ||
Annotation | intron_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000439388, ENST00000371872, ENST00000422262, ENST00000371868, ENST00000469828); non_coding_transcript_variant(ENST00000469828) | ||
SIFT Annotation | tolerated_-_low_confidence; tolerated | ||
SIFT Variant Effect | tolerated_-_low_confidence(ENST00000422262); tolerated(ENST00000371868, ENST00000371872, ENST00000439388) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000371868, ENST00000371872, ENST00000422262, ENST00000439388) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Strong transcription;Bivalent Enhancer;Enhancers | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |