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SNP Report
Name | rs12545826 dbSNP Ensembl | ||
---|---|---|---|
Location | chr8:10085397 - 10085397(1) | ||
Variant Alleles | G/C | ||
Ancestral Allele | G | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.293331 | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000317173, ENST00000441698, ENST00000518255, ENST00000521209) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |