Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.22 (C)
Location

Chromosome X:120075703 (forward strand) | View in location tab

Co-located

with dbSNP rs3764827 (A/C)

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

Variation displays