Original source

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

Alleles
-/A
Location

Chromosome X: between 83506270 and 83506271 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.83506270dupA

Variation displays