Original source

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

-/AAT | MAF: 0.40 (-)

Chromosome 5: between 162071011 and 162071012 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs146838438

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 1099 individual genotypes.

Variation displays