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SNP Report
Name | rs9807929 dbSNP Ensembl | ||
---|---|---|---|
Location | chr2:162688353 - 162688353(1) | ||
Variant Alleles | C/G/T | ||
Ancestral Allele | T | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.241414 | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000328032, ENST00000332142) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |