Original source

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

Alleles
-/GAAA/CA/AC
Location

Chromosome 7: between 101136456 and 101136457 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs139690533

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

Variation displays