Original source

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

Alleles
-/A|MAF: 0.30 (-)
Location

Chromosome X: between 83506269 and 83506270 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs369191212, rs143316333

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2512 sample genotypes.

Variant displays