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SNP Report
| Name | rs4779955 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chrCHR_HSCHR15_4_CTG8:32168640 - 32168640(1) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | G | ||
| Minor Allele | A | ||
| Minor Allele Frequence | 0.453674 | ||
| Functional Annotation | intron_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000635978, ENST00000636603, ENST00000637183, ENST00000638106) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


