Original source

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

Alleles
-/AAT | MAF: 0.40 (-)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs146838438

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

Variation displays