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SNP Report
Name | rs7250233 dbSNP Ensembl | ||
---|---|---|---|
Location | chr19:19520139 - 19520139(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.11901 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000428459, ENST00000502506, ENST00000503283, ENST00000507754, ENST00000511180, ENST00000511584, ENST00000555938, ENST00000586674, ENST00000606722); NMD_transcript_variant(ENST00000502506, ENST00000606722); non_coding_transcript_variant(ENST00000511180, ENST00000511584, ENST00000586674); upstream_gene_variant(ENST00000585580, ENST00000587522) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |