Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.01 (A)

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57358857

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 8 transcripts, has 2510 sample genotypes and is mentioned in 1 citation.

Variant displays