This variant has been flagged

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

Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

Chromosome 17:5441126 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs386513029

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 20 transcripts and has 859 sample genotypes.

Variant displays