Original source

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

Alleles
-/C | MAF: 0.06 (C)
Location

Chromosome X: between 83506303 and 83506304 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.83506303_83506304insC

Variation displays