SNP Report
Name | rs129928 dbSNP Ensembl | ||
---|---|---|---|
Location | 9:133663226 - 133663226(+) | ||
Variant Seq | A | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.226837 | ||
Annotation | downstream_gene_variant | ||
Variant Effect | downstream_gene_variant(ENST00000469828, ENST00000371872, ENST00000393056, ENST00000371868, ENST00000439388, ENST00000422262) | ||
SIFT Annotation | deleterious_-_low_confidence | ||
SIFT Variant Effect | deleterious_-_low_confidence(ENST00000393056) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000393056) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Genic enhancers;Bivalent Enhancer;Strong transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |