Original source

Variants (including SNPs and indels) imported from dbSNP (release 143)|View in dbSNP

A/G|Ambiguity code: R

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

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina BovineHD BeadChip

About this variant

This variant overlaps 3 transcripts and has 8 sample genotypes.

Variant displays