SNP Report
Name | rs16834851 dbSNP Ensembl | ||
---|---|---|---|
Location | 1:192804950 - 192804950(+) | ||
Variant Seq | G | ||
Ancestral Allele | A | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.32528 | ||
Annotation | downstream_gene_variant; upstream_gene_variant | ||
Variant Effect | downstream_gene_variant(ENST00000429211); upstream_gene_variant(ENST00000235382, ENST00000487236, ENST00000483295, ENST00000464302) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000235382) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000235382) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |