Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.02 (A)
Location

Chromosome X:3604116 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

X:g.3604116G>A

About this variant

This variant overlaps 3 transcripts and has 2508 sample genotypes.

Variant displays