SNP Report
Name | rs7754668 dbSNP Ensembl | ||
---|---|---|---|
Location | 6:35622315 - 35622315(+) | ||
Variant Seq | A | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.0457268 | ||
Annotation | intron_variant | ||
Variant Effect | intron_variant(ENST00000539068, ENST00000542713, ENST00000536438, ENST00000357266) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000536438, ENST00000357266, ENST00000542713, ENST00000539068) | ||
PolyPhen Annotation | benign; possibly_damaging | ||
PolyPhen Variant Effect | benign(ENST00000536438, ENST00000357266, ENST00000539068); possibly_damaging(ENST00000542713) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Strong transcription;Genic enhancers;Enhancers | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |