Original source

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

Alleles
-/AA/AAT
Location

Chromosome 5: between 181236638 and 181236639 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs66803184, rs66803185

This variation has 2 HGVS names - click the plus to show

Variation displays