Original source

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

Alleles
-/A
Location

Chromosome X: between 37780929 and 37780930 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 5 HGVS names - click the plus to show

Variation displays