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:135984770 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.135984770G>T

Variation displays