SNP Report
Name | rs12029329 dbSNP Ensembl | ||
---|---|---|---|
Location | 1:46414184 - 46414184(+) | ||
Variant Seq | G | ||
Ancestral Allele | G | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.294329 | ||
Annotation | downstream_gene_variant | ||
Variant Effect | downstream_gene_variant(ENST00000243167, ENST00000484697, ENST00000493735, ENST00000493636, ENST00000489366) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000243167) | ||
PolyPhen Annotation | possibly_damaging | ||
PolyPhen Variant Effect | possibly_damaging(ENST00000243167) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Weak transcription;Strong transcription;Enhancers | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |