This variant has been flagged

None of the variant alleles match the reference allele (A)

Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: A | Ambiguity code: Y
Note: The reference base for this variant (C) does not match the Ensembl reference base (A) at this location.
Location

Chromosome 2:104854218 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 3 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 14 transcripts and 1 regulatory feature.

Variant displays