Original source

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

Alleles
-/G | MAF: 0.31 (-)
Location

Chromosome X: between 83506268 and 83506269 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.83506268_83506269insG

Variation displays