Original source

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

Alleles
-/G
Location

Chromosome X: between 83506301 and 83506302 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

X:g.83506301_83506302insG

Variation displays