Original source

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

Alleles
A/G | Ambiguity code: R
Location

Chromosome X:153446969 (forward strand) | View in location tab

Co-located

with dbSNP rs62617800 (A/G)

Most severe consequence
Evidence status

HGVS name

X:g.153446969A>G

Variation displays