SNP Report
Name | rs7928213 dbSNP Ensembl | ||
---|---|---|---|
Location | 11:34466738 - 34466738(+) | ||
Variant Seq | A | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.263578 | ||
Annotation | downstream_gene_variant; upstream_gene_variant; intron_variant; non_coding_transcript_variant | ||
Variant Effect | downstream_gene_variant(ENST00000530343); upstream_gene_variant(ENST00000534710); intron_variant(ENST00000525707, ENST00000241052); non_coding_transcript_variant(ENST00000525707) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000241052) | ||
PolyPhen Annotation | probably_damaging | ||
PolyPhen Variant Effect | probably_damaging(ENST00000241052) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | TF binding region | ||
Chromatin State | Weak transcription;ZNF genes & repeats;Strong transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |