Original source

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

Alleles
G/T|Ancestral: T|Ambiguity code: K|MAF: 0.38 (G)
Location

Chromosome X:43731789 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM073190

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms
HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 3 transcripts, has 3802 sample genotypes, is associated with 1 phenotype and is mentioned in 23 citations.

Variant displays