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SNP Report
Name | rs10888778 dbSNP Ensembl | ||
---|---|---|---|
Location | chr1:53269774 - 53269774(1) | ||
Variant Alleles | G/T | ||
Ancestral Allele | T | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.372804 | ||
Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000432653); intron_variant(ENST00000306052, ENST00000347547, ENST00000354412, ENST00000371454, ENST00000465675, ENST00000475501, ENST00000480045); NMD_transcript_variant(ENST00000480045); upstream_gene_variant(ENST00000459674, ENST00000481431) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |