Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP


Chromosome 17: between 42907562 and 42907563 (forward strand) | View in location tab

Most severe consequence
Frameshift variant
Evidence status

Clinical significance


LSDB NM_000151.2:c.379_380dupTA

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, is associated with 3 phenotypes and is mentioned in 2 citations.

Variant displays