SNP Report
Name | rs2148269 dbSNP Ensembl | ||
---|---|---|---|
Location | 10:24894003 - 24894003(+) | ||
Variant Seq | G | ||
Ancestral Allele | A | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.206869 | ||
Annotation | intron_variant | ||
Variant Effect | intron_variant(ENST00000320152, ENST00000376378) | ||
SIFT Annotation | deleterious_-_low_confidence | ||
SIFT Variant Effect | deleterious_-_low_confidence(ENST00000376376) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000376376) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Enhancers;Strong transcription | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature |