Original source

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

Alleles
-/T
Location

Chromosome 18: between 5392252 and 5392253 (forward strand) | View in location tab

Most severe consequence
HGVS name

18:g.5392252_5392253insT

About this variant

This variant overlaps 12 transcripts.

Variation displays