Original source

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


Chromosome 16: between 50755145 and 50755146 (forward strand) | View in location tab

Most severe consequence
Intron variant

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts.

Variant displays