Original source

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

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

Chromosome X:48686261 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57358857

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 6 individual genotypes and is mentioned in 1 citation.

Variation displays