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SNP Report
Name | rs2304512 dbSNP Ensembl | ||
---|---|---|---|
Location | chr3:51388050 - 51388050(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.147364 | ||
Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000266037); intron_variant(ENST00000446668, ENST00000470900, ENST00000482262, ENST00000528157); NMD_transcript_variant(ENST00000446668); non_coding_transcript_variant(ENST00000470900, ENST00000482262); upstream_gene_variant(ENST00000563281) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |