Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

AACTT/- | MAF: 0.26 (-)

Chromosome 4:54227623-54227627 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs144906182

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 1096 individual genotypes.

Variation displays