SNP Report
Name | rs2214837 dbSNP Ensembl | ||
---|---|---|---|
Location | 7:30634164 - 30634164(+) | ||
Variant Seq | G | ||
Ancestral Allele | A | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.399561 | ||
Annotation | downstream_gene_variant | ||
Variant Effect | downstream_gene_variant(ENST00000496643, ENST00000485784, ENST00000389266, ENST00000444666, ENST00000465748, LRG_243t1) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000389266, ENST00000444666, LRG_243t1) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000389266, ENST00000444666, LRG_243t1) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Strong transcription;Weak transcription;Genic enhancers;Enhancers | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |