Original source

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

A/G|Ambiguity code: R

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

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 1 sample genotype.

Variant displays