Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.09 (G)
Location

Chromosome X:120431026 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61558404, rs3174395

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

This variation has assays on 7 chips - click the plus to show

Variation displays