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SNP Report
Name | rs13014266 dbSNP Ensembl | ||
---|---|---|---|
Location | chr2:166457394 - 166457394(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.446486 | ||
Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000497562); intron_variant(ENST00000409855, ENST00000419992, ENST00000424326, ENST00000441411, ENST00000619410, ENST00000621965); NMD_transcript_variant(ENST00000424326) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |