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:100988470 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Archive dbSNP rs60295890

This variant has 7 HGVS names - click the plus to show

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 1204 sample genotypes.

Variant displays