SNP Report
Name | rs2039988 dbSNP Ensembl | ||
---|---|---|---|
Location | 1:238411180 - 238411180(+) | ||
Variant Seq | C | ||
Ancestral Allele | C | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.150958 | ||
Annotation | upstream_gene_variant | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000611898, ENST00000366570) | ||
PolyPhen Annotation | unknown | ||
PolyPhen Variant Effect | unknown(ENST00000604646) | ||
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 |