Original source

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

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

Chromosome X: between 41514603 and 41514604 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.41514603_41514604insC

Variation displays