Original source

Variants (including SNPs and indels) imported from dbSNP (release 140) | [View in dbSNP]

A/C/G | Ambiguity code: V

Chromosome X:92296528 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 4 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina BovineHD BeadChip

About this variant

This variant overlaps 6 transcripts.

Variation displays