Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome X:2953163 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980122, CM950100

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

About this variant

This variant overlaps 10 transcripts, is associated with 3 phenotypes and is mentioned in 5 citations.

Variation displays