Original source

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

Alleles
T/A | Ambiguity code: W
Location

Chromosome X:153446801 (forward strand) | View in location tab

Co-located

with dbSNP rs2968488 (A/T)

Most severe consequence
HGVS name

X:g.153446801T>A

Variation displays