Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.08 (A)

Chromosome X:83509032 (forward strand) | View in location tab


with COSMIC COSM4157035 (A/G), COSM4157034 (A/G) ; dbSNP rs111919890 (A/-)

Most severe consequence
Evidence status

Clinical significance


Archive dbSNP rs58335216

This variation has 3 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 1496 individual genotypes and is associated with 1 phenotype.

Variation displays