SNP Report
Name | rs2174444 dbSNP Ensembl | ||
---|---|---|---|
Location | 5:76969697 - 76969697(+) | ||
Variant Seq | T | ||
Ancestral Allele | C | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.425519 | ||
Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant | ||
Variant Effect | downstream_gene_variant(ENST00000274368, ENST00000503763); intron_variant(ENST00000514258); non_coding_transcript_variant(ENST00000514258) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000274368) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000274368) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Strong transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |