SNP Report
Name | rs11514279 dbSNP Ensembl | ||
---|---|---|---|
Location | 12:68129579 - 68129579(+) | ||
Variant Seq | T | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.126997 | ||
Annotation | intron_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000536914); non_coding_transcript_variant(ENST00000536914) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000393555, ENST00000344096) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000393555, ENST00000344096) | ||
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 |