Original source

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

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

Chromosome X:43678961 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61677452, rs56419047

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

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 750 sample genotypes and is mentioned in 6 citations.

Variant displays