SNP Report
Name | rs62054824 dbSNP Ensembl | ||
---|---|---|---|
Location | 17:45852626 - 45852626(+) | ||
Variant Seq | T | ||
Ancestral Allele | T | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.086262 | ||
Annotation | intron_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000579599, ENST00000579244, ENST00000634876); non_coding_transcript_variant(ENST00000579599, ENST00000579244, ENST00000634876) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000329196) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000329196) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Weak transcription;Enhancers;Flanking Active TSS | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |