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SNP Report
Name | rs10860861 dbSNP Ensembl | ||
---|---|---|---|
Location | chr12:102391791 - 102391791(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | T | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.458267 | ||
Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000337514, ENST00000456098); intron_variant(ENST00000635615); non_coding_transcript_exon_variant(ENST00000626826); non_coding_transcript_variant(ENST00000626826, ENST00000635615) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |