Original source

Variants (including SNPs and indels) imported from dbSNP (release 139) | View in dbSNP

Alleles
A/G | Ambiguity code: R
Location

Chromosome X1:20711138 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 1 individual genotype.

Variation displays