SNP Report
Name | rs853175 dbSNP Ensembl | ||
---|---|---|---|
Location | 5:143257225 - 143257225(+) | ||
Variant Seq | C | ||
Ancestral Allele | C | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.384385 | ||
Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000378004, ENST00000418236, ENST00000443674, ENST00000274498) | ||
PolyPhen Annotation | benign; possibly_damaging | ||
PolyPhen Variant Effect | benign(ENST00000378004, ENST00000418236); possibly_damaging(ENST00000443674, ENST00000274498) | ||
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 |