Original source

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

G/A/T | Ancestral: T | Ambiguity code: D | MAF: 0.01 (G)

Chromosome X:154766321 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


Archive dbSNP rs17850576, rs17850605

HGVS names

This variant has 29 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 28 transcripts, has 2509 sample genotypes and is associated with 1 phenotype.

Variant displays