Original source

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

Alleles
G/-/TG
Location

Chromosome X:49706554 (forward strand) | View in location tab

Co-located

with dbSNP rs67728963 (G/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs200567650, rs57183198

This variation has 8 HGVS names - click the plus to show

Variation displays