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SNP Report
| Name | rs4822360 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr22:23140273 - 23140273(1) | ||
| Variant Alleles | A/G/T | ||
| Ancestral Allele | G | ||
| Minor Allele | A | ||
| Minor Allele Frequence | 0.47524 | ||
| Functional Annotation | missense_variant; synonymous_variant; upstream_gene_variant.
Polyphen Annotation: probably damaging(ENST00000216036, ENST00000406876, ENST00000452757) SIFT Annotation: deleterious(ENST00000216036, ENST00000406876, ENST00000452757) |
||
| Consequence to Transcript | missense_variant(ENST00000216036, ENST00000406876, ENST00000452757); synonymous_variant(ENST00000216036, ENST00000406876, ENST00000452757); upstream_gene_variant(ENST00000439064, ENST00000459276) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


