SNP Report
Name | rs2747736 dbSNP Ensembl | ||
---|---|---|---|
Location | 6:99005829 - 99005829(+) | ||
Variant Seq | T | ||
Ancestral Allele | C | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.156949 | ||
Annotation | upstream_gene_variant | ||
SIFT Annotation | deleterious_-_low_confidence | ||
SIFT Variant Effect | deleterious_-_low_confidence(ENST00000229971, ENST00000369244) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000229971, ENST00000369244) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Enhancers | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |