Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome X:100987316 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs6620969, rs59954872

This variation has 4 HGVS names - click the plus to show

This variation has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 1185 individual genotypes.

Variation displays