Original source

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

Alleles
T/A | Ancestral: A | Ambiguity code: W
Location

Chromosome X:154181312 (forward strand) | View in location tab

Co-located

with dbSNP rs2968488 (A/T)

Most severe consequence
HGVS name

X:g.154181312T>A

Variation displays