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SNP Report
Name | rs13081028 dbSNP Ensembl | ||
---|---|---|---|
Location | chr3:52521300 - 52521300(1) | ||
Variant Alleles | G/A | ||
Ancestral Allele | A | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.454473 | ||
Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000307076, ENST00000422318, ENST00000459839, ENST00000461325, ENST00000462261, ENST00000463947, ENST00000466112, ENST00000469616, ENST00000478091, ENST00000479024, ENST00000492555); intron_variant(ENST00000321725, ENST00000481626); non_coding_transcript_variant(ENST00000481626); upstream_gene_variant(ENST00000462681, ENST00000462741, ENST00000469989) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |