Original source

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

Alleles
-/AC/CA
Location

Chromosome 7: between 101136457 and 101136458 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59199672

This variation has 4 HGVS names - click the plus to show

Variation displays