Original source

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

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

Chromosome X: between 41373856 and 41373857 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.41373856_41373857insC

Variation displays