
SNP Report
Name | rs12049330 dbSNP Ensembl |
---|---|
Location | Chrchr1:110031188(Forward) |
Variant Alleles | T/G |
Ancestral Allele | T |
Annotation | intron_variant; nc_transcript_variant; upstream_gene_variant |
Consequence to Transcript | intron_variant(ENST00000369870, ENST00000463678, ENST00000497545) nc_transcript_variant(ENST00000463678, ENST00000497545) upstream_gene_variant(ENST00000369869, ENST00000459635) |
No. of Studies (Positive/Negative) | 1 (0/1)
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