
SNP Report
Name | rs1526285 dbSNP Ensembl |
---|---|
Location | Chrchr2:150508525(Forward) |
Variant Alleles | C/A |
Ancestral Allele | C |
Annotation | intron_variant; nc_transcript_variant |
Consequence to Transcript | intron_variant(ENST00000449714) nc_transcript_variant(ENST00000449714) |
No. of Studies (Positive/Negative) | 1 (0/1)
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