SNP Report
Name | rs10249885 dbSNP Ensembl | ||
---|---|---|---|
Location | 7:30622621 - 30622621(+) | ||
Variant Seq | A | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.404353 | ||
Annotation | downstream_gene_variant; non_coding_transcript_exon_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant | ||
Variant Effect | downstream_gene_variant(ENST00000484093); non_coding_transcript_exon_variant(ENST00000478124); intron_variant(ENST00000389266, ENST00000444666, ENST00000470392, LRG_243t1); NMD_transcript_variant(ENST00000444666); non_coding_transcript_variant(ENST00000478124, ENST00000470392) | ||
SIFT Annotation | deleterious; tolerated | ||
SIFT Variant Effect | deleterious(ENST00000444666); tolerated(LRG_243t1, ENST00000389266) | ||
PolyPhen Annotation | benign; probably_damaging | ||
PolyPhen Variant Effect | benign(LRG_243t1, ENST00000389266); probably_damaging(ENST00000444666) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Weak transcription;Strong transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |