Original source

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


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

Most severe consequence
Non coding transcript exon variant

Archive dbSNP rs369191212, rs143316333

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

About this variant

This variant overlaps 2 transcripts and has 8 sample genotypes.

Variant displays