Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome X:37803981 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

This variant has 6 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 447 sample genotypes.

Variant displays