Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome X:48528641 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3189604

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 2 individual genotypes.

Variation displays