Original source

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


Chromosome 5: between 132390839 and 132390840 (forward strand) | View in location tab

Most severe consequence
Stop gained
Evidence status


LSDB SCV000111943, 11838

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays