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