This variant has been flagged

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

Original source

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

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

Chromosome 4:3074415 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386601835

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature and has 2 sample genotypes.

Variant displays