Original source

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

Alleles
-/A
Location

Chromosome 4: between 89794716 and 89794717 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs72624321, rs72614928

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

Variation displays