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SNP Report
Name | rs12995487 dbSNP Ensembl | ||
---|---|---|---|
Location | chr2:159392606 - 159392606(1) | ||
Variant Alleles | C/G | ||
Ancestral Allele | C | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.230232 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000294905, ENST00000392782, ENST00000392783, ENST00000420020, ENST00000551504); non_coding_transcript_variant(ENST00000420020, ENST00000551504); upstream_gene_variant(ENST00000485917, ENST00000594921, ENST00000608714, ENST00000626302) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |