Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.02 (G)
Location

Chromosome X:120425733 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2506 sample genotypes.

Variant displays