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:134458434 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.134458434G>T

Variation displays