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SNP Report
| Name | rs11939575 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr4:186706638 - 186706638(1) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | C | ||
| Minor Allele | T | ||
| Minor Allele Frequence | 0.254193 | ||
| Functional Annotation | downstream_gene_variant; missense_variant.
Polyphen Annotation: benign(ENST00000441802, ENST00000614102) SIFT Annotation: tolerated(ENST00000441802, ENST00000614102) |
||
| Consequence to Transcript | downstream_gene_variant(ENST00000509647); missense_variant(ENST00000441802, ENST00000614102) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


