SNP Report
Name | rs6602398 dbSNP Ensembl | ||
---|---|---|---|
Location | 10:6040990 - 6040990(+) | ||
Variant Seq | T | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.161342 | ||
Annotation | downstream_gene_variant; intron_variant | ||
Variant Effect | downstream_gene_variant(ENST00000440436); intron_variant(ENST00000379954, LRG_73t1, ENST00000256876, ENST00000379959) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(LRG_73t1, ENST00000447847, ENST00000379959, ENST00000379954, ENST00000256876) | ||
PolyPhen Annotation | probably_damaging | ||
PolyPhen Variant Effect | probably_damaging(LRG_73t1, ENST00000447847, ENST00000379959, ENST00000379954, ENST00000256876) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Enhancers;Genic enhancers | ||
No. of Marker's Association Results | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature |
The LD data used here is based on 1000 Genome Phase I. LD SNP pairs were selected with a threshold r2<=0.8.