Original source

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

Alleles
CAGT/-
Location

Chromosome X:136167097-136167100 (forward strand) | View in location tab

Most severe consequence

This variation has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 23 transcripts and has 1 individual genotype.

Variation displays