SNP Report
Name | rs10762479 dbSNP Ensembl | ||
---|---|---|---|
Location | 10:51897888 - 51897888(+) | ||
Variant Seq | G | ||
Ancestral Allele | G | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.306909 | ||
Annotation | intron_variant | ||
Variant Effect | intron_variant(ENST00000401604, ENST00000373980, ENST00000373985, ENST00000373976) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000373980, ENST00000401604, ENST00000373985, ENST00000373976) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000373980, ENST00000401604, ENST00000373985, ENST00000373976) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Enhancers;Weak transcription | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature |