SNP Report
Name | rs17763634 dbSNP Ensembl | ||
---|---|---|---|
Location | 17:45844388 - 45844388(+) | ||
Variant Seq | C | ||
Ancestral Allele | T | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.0860623 | ||
Annotation | upstream_gene_variant; intron_variant; non_coding_transcript_variant | ||
Variant Effect | upstream_gene_variant(ENST00000329196); intron_variant(ENST00000579244, ENST00000579599, ENST00000634876, ENST00000581125); non_coding_transcript_variant(ENST00000579244, ENST00000579599, ENST00000634876, ENST00000581125) | ||
SIFT Annotation | deleterious_-_low_confidence | ||
SIFT Variant Effect | deleterious_-_low_confidence(ENST00000329196) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000329196) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |