Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

A/T | Ancestral: T | Ambiguity code: W | MAF: 0.27 (T)

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17312213, rs59912223

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2832 sample genotypes.

Variant displays