Original source

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

Alleles
-/T | MAF: 0.11 (T)
Location

Chromosome X: between 41514599 and 41514600 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs201295146

HGVS name

X:g.41514599_41514600insT

Variation displays