Original source

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

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

Chromosome X:43744144 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 4 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 1564 individual genotypes and is mentioned in 21 citations.

Variation displays