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SNP Report
| Name | rs10017784 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr4:52628649 - 52628649(1) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | G | ||
| Minor Allele | G | ||
| Minor Allele Frequence | 0.19369 | ||
| Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000504078); intron_variant(ENST00000441222, ENST00000451218, ENST00000503060, ENST00000506707, ENST00000508499, ENST00000512656, ENST00000514536); NMD_transcript_variant(ENST00000503060, ENST00000512656, ENST00000514536); non_coding_transcript_variant(ENST00000506707); upstream_gene_variant(ENST00000502443) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


