Original source

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

Alleles
-/ATAC | MAF: 0.15 (ATAC)
Location

Chromosome X: between 46911428 and 46911429 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.46911428_46911429insATAC

Variation displays