Original source

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

Alleles
TTG/-
Location

Chromosome X:151398409-151398411 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs146948708

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 1 sample genotype.

Variant displays