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SNP Report
| Name | rs12488461 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr3:52664401 - 52664401(1) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | T | ||
| Minor Allele | C | ||
| Minor Allele Frequence | 0.311302 | ||
| Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000449505, ENST00000450271); intron_variant(ENST00000296302, ENST00000337303, ENST00000356770, ENST00000394830, ENST00000409057, ENST00000409114, ENST00000409767, ENST00000410007, ENST00000412587, ENST00000420148, ENST00000423351, ENST00000431678, ENST00000446103); NMD_transcript_variant(ENST00000412587) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


