Original source

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

Alleles
G/-/TG | Ancestral: G
Location

Chromosome X:49941944 (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