Original source

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

Alleles
AA/-/A
Location

Chromosome 14:92104939-92104940 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58000789

This variation has 100 HGVS names - click the plus to show

Variation displays