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SNP Report
Name | rs12680389 dbSNP Ensembl | ||
---|---|---|---|
Location | chr8:10099347 - 10099347(1) | ||
Variant Alleles | G/C | ||
Ancestral Allele | G | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.253594 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000317173, ENST00000382490, ENST00000441698, ENST00000518255, ENST00000521209, ENST00000522907, ENST00000523637, ENST00000528246); non_coding_transcript_variant(ENST00000523637) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |