Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome X:48523824 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM030033

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_090_EBP_300205_0013, 6924

This variation has 9 HGVS names - click the plus to show

Variation displays