Original source

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

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

Chromosome X:48523775 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3174404

This variation has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 2 individual genotypes.

Variation displays