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

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.

Chromosome 6:43621640 (forward strand)|View in location tab

Most severe consequence
Missense variant
Evidence status


Archive dbSNP rs386561872

HGVS names

This variant has 18 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 22 transcripts and has 263 sample genotypes.

Variant displays