SNP Report
Name | rs7929974 dbSNP Ensembl | ||
---|---|---|---|
Location | 11:75318123 - 75318123(+) | ||
Variant Seq | T | ||
Ancestral Allele | C | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.446286 | ||
Annotation | intron_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000533255, ENST00000420843, ENST00000360025); non_coding_transcript_variant(ENST00000533255) | ||
SIFT Annotation | tolerated_-_low_confidence | ||
SIFT Variant Effect | tolerated_-_low_confidence(ENST00000532525) | ||
PolyPhen Annotation | unknown | ||
PolyPhen Variant Effect | unknown(ENST00000527385) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Enhancers;Weak transcription;Genic enhancers;Strong transcription | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature |
The LD data used here is based on 1000 Genome Phase I. LD SNP pairs were selected with a threshold r2<=0.8.