SNP Report
Name | rs11177074 dbSNP Ensembl | ||
---|---|---|---|
Location | 12:68150654 - 68150654(+) | ||
Variant Seq | C | ||
Ancestral Allele | T | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.141573 | ||
Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant | ||
Variant Effect | downstream_gene_variant(ENST00000229135); intron_variant(ENST00000536914); non_coding_transcript_variant(ENST00000536914) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000229135) | ||
PolyPhen Annotation | probably_damaging | ||
PolyPhen Variant Effect | probably_damaging(ENST00000229135) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |