Original source

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

Alleles
-/T
Location

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

Most severe consequence
Synonyms

Archive dbSNP rs201295146

HGVS name

X:g.41514599_41514600insT

About this variant

This variant overlaps 4 transcripts and has 1 individual genotype.

Variation displays