Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/A
Location

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

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Synonyms

Archive dbSNP rs369191212, rs143316333

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 8 individual genotypes.

Variation displays