Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.42 (A)
Location

Chromosome X:43678769 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17310595

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, has 2755 sample genotypes and is mentioned in 3 citations.

Variant displays