SNP Report
Name | rs61882275 dbSNP Ensembl | ||
---|---|---|---|
Location | 11:34482745 - 34482745(+) | ||
Variant Seq | A | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.366613 | ||
Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant | ||
Variant Effect | downstream_gene_variant(ENST00000579311); intron_variant(ENST00000429939, ENST00000257832, ENST00000620316, ENST00000528709, ENST00000312319); non_coding_transcript_variant(ENST00000528709) | ||
SIFT Annotation | deleterious; tolerated | ||
SIFT Variant Effect | deleterious(ENST00000312319, ENST00000257832, ENST00000429939); tolerated(ENST00000620316) | ||
PolyPhen Annotation | probably_damaging; possibly_damaging | ||
PolyPhen Variant Effect | probably_damaging(ENST00000620316); possibly_damaging(ENST00000312319, ENST00000257832, ENST00000429939) | ||
rSNP? | No Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Inactive region | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |