Original source

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

C/G/T | Ancestral: G | Ambiguity code: B | MAF: < 0.01 (G)

Chromosome X:136145045 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 20 transcripts and has 2504 sample genotypes.

Variant displays