Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


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