SNP Report
Name | rs2134655 dbSNP Ensembl | ||
---|---|---|---|
Location | 3:114139354 - 114139354(+) | ||
Variant Seq | T | ||
Ancestral Allele | C | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.203275 | ||
Annotation | intron_variant | ||
Variant Effect | intron_variant(ENST00000460779, ENST00000295881, ENST00000383673, ENST00000467632) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000295881, ENST00000383673, ENST00000467632, ENST00000460779) | ||
PolyPhen Annotation | benign; probably_damaging | ||
PolyPhen Variant Effect | benign(ENST00000295881); probably_damaging(ENST00000383673, ENST00000467632, ENST00000460779) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Enhancers | ||
No. of Marker's Association Results | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature |