Original source

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

Alleles
-/AAT | MAF: 0.21 (AAT)
Location

Chromosome 5: between 181236637 and 181236638 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs140642872

HGVS name

5:g.181236637_181236638insAAT

Variation displays