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SNP Report
Name | rs2193923 dbSNP Ensembl | ||
---|---|---|---|
Location | chr2:159441612 - 159441612(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.28734 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000343439, ENST00000392782, ENST00000392783, ENST00000467184, ENST00000482503); non_coding_transcript_variant(ENST00000467184, ENST00000482503); upstream_gene_variant(ENST00000605196) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |