Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

G/A|Ancestral: G|Ambiguity code: R|MAF: < 0.01 (A)

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

Co-located variant

dbSNP rs111919890 (-/A)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


Archive dbSNP rs58335216

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 2 transcripts, has 2893 sample genotypes and is associated with 1 phenotype.

Variant displays