Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

-/A | MAF: 0.28 (-)

Chromosome X: between 83506269 and 83506270 (forward strand) | View in location tab

Most severe consequence

Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]

Evidence status


Archive dbSNP rs369191212, rs143316333

This variation has 2 HGVS names - click the plus to show

Variation displays