SNP Report
Name | rs152313 dbSNP Ensembl | ||
---|---|---|---|
Location | 5:56232440 - 56232440(+) | ||
Variant Seq | A | ||
Ancestral Allele | A | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.423722 | ||
Annotation | intron_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000519114, ENST00000513241, ENST00000504958, ENST00000341048); non_coding_transcript_variant(ENST00000519114) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000341048, ENST00000504958) | ||
PolyPhen Annotation | benign; possibly_damaging | ||
PolyPhen Variant Effect | benign(ENST00000504958); possibly_damaging(ENST00000341048) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Active TSS;Enhancers | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |