SNP Report
Name | rs4814437 dbSNP Ensembl | ||
---|---|---|---|
Location | 20:16157294 - 16157294(+) | ||
Variant Seq | A | ||
Ancestral Allele | A | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.474042 | ||
Annotation | downstream_gene_variant | ||
SIFT Annotation | deleterious_-_low_confidence; deleterious | ||
SIFT Variant Effect | deleterious_-_low_confidence(ENST00000407045); deleterious(ENST00000378058, ENST00000402914) | ||
PolyPhen Annotation | possibly_damaging; probably_damaging | ||
PolyPhen Variant Effect | possibly_damaging(ENST00000407045); probably_damaging(ENST00000378058, ENST00000402914) | ||
rSNP? | No Link in rVarBase | ||
Related Regulatory Elements | N.A. | ||
Chromatin State | N.A. | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |