Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

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

Most severe consequence
Evidence status

HGVS name

X:g.3604116G>A

About this variant

This variant overlaps 3 transcripts and has 4 individual genotypes.

Variation displays