Original source

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

Alleles
C/A/G | Ancestral: C | Ambiguity code: V
Location

Chromosome X:2871204 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM950100, CM980122

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 20 HGVS names - click the plus to show

Variation displays