Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome X:135984769 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.135984769G>T

This variation has assays on 5 chips - click the plus to show

Variation displays