Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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