SNP Report
Name | rs3935637 dbSNP Ensembl | ||
---|---|---|---|
Location | 17:45851207 - 45851207(+) | ||
Variant Seq | C | ||
Ancestral Allele | C | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.351837 | ||
Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant | ||
Variant Effect | downstream_gene_variant(ENST00000329196); intron_variant(ENST00000634876, ENST00000579244, ENST00000579599); non_coding_transcript_variant(ENST00000634876, ENST00000579244, ENST00000579599) | ||
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 | Enhancers;Weak transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |