Original source

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

Alleles
-/G | MAF: 0.01 (G)
Location

Chromosome X: between 136145604 and 136145605 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.136145604_136145605insG

Variation displays