Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome X:19355713 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920573, CM084910

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 7528, 25917

This variation has 11 HGVS names - click the plus to show

Variation displays