Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome X:151399780 (forward strand) | View in location tab

Co-located

with dbSNP rs200496040 (T/C)

Most severe consequence
Evidence status

Synonyms

This variation has 4 HGVS names - click the plus to show

Variation displays