Original source

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

A/G | Ambiguity code: R

Chromosome X:101049495 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17348367

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 1 sample genotype.

Variant displays