Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K
Location

Chromosome X:46998874 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59286713, rs17323126

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 315 individual genotypes.

Variation displays