This variant has been flagged

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

Original source

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

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

Chromosome 7:44062847 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Archive dbSNP rs3187852, rs386518021

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 48 transcripts and has 272 sample genotypes.

Variant displays