Original source

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

Alleles
-/A | MAF: 0.28 (-)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs369191212, rs143316333

HGVS name

X:g.83506269_83506270insA

Variation displays