Original source

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


Chromosome 19: between 5830625 and 5830626 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs386388441

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 24 transcripts and has 1 individual genotype.

Variation displays