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SNP Report
Name | rs12988336 dbSNP Ensembl | ||
---|---|---|---|
Location | chr2:159449408 - 159449408(1) | ||
Variant Alleles | A/C | ||
Ancestral Allele | C | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.259815 | ||
Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000605196); intron_variant(ENST00000343439, ENST00000392782, ENST00000392783, ENST00000437839, ENST00000467184, ENST00000482503, ENST00000541068); non_coding_transcript_variant(ENST00000467184, ENST00000482503) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |