Original source

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

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

Chromosome X:153994204 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990477

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 13 HGVS names - click the plus to show

Variation displays