Original source

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

Alleles
A/-/AA/AAAA | Ancestral: A
Location

Chromosome 6:144062495 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs71881634, rs61024620

This variation has 12 HGVS names - click the plus to show

Variation displays