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

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

Chromosome 10:6011919 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs386525830

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 8 transcripts and has 47 sample genotypes.

Variant displays