SNP Report
Name | rs2070744 dbSNP Ensembl |
---|---|
Location | Chrchr7:150690079(Forward) |
Variant Alleles | C/T |
Ancestral Allele | C |
Annotation | intron_variant; upstream_gene_variant |
Consequence to Transcript | intron_variant(ENST00000297494, ENST00000461406, ENST00000484576) upstream_gene_variant(ENST00000467517, ENST00000484524) |
No. of Studies (Positive/Negative) | 1 (0/1) |