Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.40 (T)
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 2667 individual genotypes, is associated with 1 phenotype and is mentioned in 18 citations.

Variation displays