Original source

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

Alleles
A/T | Ancestral: T | Ambiguity code: W
Location

Chromosome X:72677453 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17312213, rs59912223

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 328 sample genotypes.

Variant displays